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CANIS LUPUS FAMILIARIS SKIN (ALK-Abello, Inc.)

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INJECTION, SOLUTION 10 mL in 1 VIAL, MULTI-DOSE (0268-0615-10) Label Information
INJECTION, SOLUTION 50 mL in 1 VIAL, MULTI-DOSE (0268-0615-50) Label Information

Complete CANIS LUPUS FAMILIARIS SKIN Information

  • BOXED WARNING(What is this?)

    WARNING

    This product is intended for use by physicians who are experienced in the administration of allergenic extracts and the emergency care of anaphylaxis or for use under the guidance of an allergy specialist.

    Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact he physician's office if reaction symptoms occur. As with all allergenic extracts, severe systemic reactions may occur. In certain individuals, these reactions may rarely result in death. Patients should be observed for 20 to 30 minutes following treatment, and emergency measures, as well as personnel trained in their use, should be immediately available in the event of a life-threatening reaction. Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk. Adverse events are to be reported to Med Watch (1-800 FDA-1088), Adverse Experience Reporting , Food and Drug Administration, , Rockville, MD 20852-9787.

    This product should not be injected intravenously. Deep subcutaneous routes have proven to be safe. Patients receiving beta-blockers may not be responsive to epinephrine or inhaled bronchodilators. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require theophylline, oxygen, intubation and the use of life support systems. Parenteral fluid and/or plasma expanders may be utilized for the treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously.

    Refer to WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS sections below.

         


  •      

    DIRECTIONS FOR USE OF
    THERAPEUTIC
    ALLERGENIC EXTRACTS


  • DESCRIPTION

    Sterile therapeutic extracts are supplied in either Phenol Saline Diluent or in Diluent containing Glycerin 50% (v/v) for subcutaneous injection. Inactive ingredients may include: Sodium Chloride for isotonicity, Glycerin, and Sodium Bicarbonate as buffering agents. Inactive ingredients in mold extracts may include residual: Potassium Phosphate, Citrate, Magnesium Phosphate and Calcium Carbonate from growth media. These products are compounded and diluted on a w/v or PNU basis.

    Pollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and, after final packaging, they are tested for sterility and safety.

    Molds are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously.

    Miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline, filtered aseptically and after final packaging are tested for sterility and safety.


  • CLINICAL PHARMACOLOGY

    The treatment consists of the subcutaneous injection of gradually increasing doses of the allergens to which the patient is allergic. It has been demonstrated that this method of treatment induces an increased tolerance to the allergens responsible for the symptoms on subsequent exposure. The exact relationships between allergen, skin-sensitizing antibody (IgE) and the blocking antibody (IgG) have not been precisely established. Clinically confirmed immunological studies have adduced evidence of the efficacy of hyposensitization therapy.

    Numerous controlled studies have demonstrated the clinical efficacy of immunotherapy with cat, dust mites and some pollen extracts. Nevertheless, responses are variable, and in a few studies patients reported no appreciable benefit.

    Extracts containing Short Ragweed pollen bear a labeled potency declaration in terms of Antigen E content. Numerous studies have confirmed Antigen E (AgE) as the major antigen associated with Short Ragweed pollinosis.1 Therefore, it is essential that the physician be aware of AgE content of allergenic extract administered for hyposensitization therapy.

    Some studies have indicated that for most patients a cumulative Antigen E dosage of less than 0.1 units is not immunizing (sufficient to stimulate specific IgG antibodies.)2 This, however, does not suggest that 0.1 unit is a maximum tolerated dose. Most moderately sensitive patients may tolerate a dosage of ten to fifty times greater. If results with this product are unsatisfactory with exquisitely sensitive patients who cannot tolerate an immunizing dose, the physician should consider alternative therapy.

    One well-controlled study demonstrated that standard immunotherapy (gradually increasing doses of antigen given subcutaneously to a maximum tolerated peak dose), using crude ragweed extract of known Antigen E potency, was significantly superior to placebo and low dose immunotherapy ( 0.1 units AgE cumulative dose) in amelioration of symptoms associated with ragweed hay fever. These patients received a cumulative dose of 18-350 units Antigen E (median = 84.9 units). The maximum single dose ranged from 3.7 to 46.8 units (median = 11.1 units) prior to the ragweed hay fever season10.

    Patients for this study were sensitive to Ragweed Antigen E, as determined by intradermal skin testing at a dose 0.01 units AgE/mL. A series of 24 weekly injections were administered. Forty-seven percent of the patients experienced at least one systemic reaction with an average of 1.2 systemic reactions per patient. None of the patients were able to achieve the expected maximum dose (90 units of Antigen E) in the 24 weekly injection dosage schedule.


  • INDICATIONS AND USAGE

    Hyposensitization (injection) therapy is a treatment for patients exhibiting allergic reactions to seasonal pollens, dust, molds, animal dander, various other inhalants, and in situations where the offending allergen cannot be avoided.

    Prior to initiation of therapy, the clinical sensitivity should be established by careful evaluation of the patient's history confirmed by diagnostic skin testing. Hyposensitization should not be prescribed for sensitivities to allergens which can easily be avoided.


  • CONTRAINDICATIONS

    A patient should not be immunized with preparations of allergens to which the patient has not demonstrated symptoms, IgE antibodies, positive skin tests, or properly controlled challenge testing. In most cases, immunotherapy is not indicated for those allergens that can be eliminated or minimized by environmental control.

    Patients on beta-blockers are not candidates for immunotherapy, as they can be non-responsive to beta-agonists that may be required to reverse a systemic reaction (also see WARNINGS AND ADVERSE REACTIONS).

    In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indication of immunotherapy must be weighed carefully against the risk of temporarily aggravating the symptoms by the injection itself.

    Also, there is some evidence, although inconclusive, that routine immunizations may exacerbate autoimmune diseases.3, 4, 5 Hyposensitization should be given cautiously to patients with this predisposition. Patients with severe cardiorespiratory symptoms are at an additional risk during a systemic reaction. The physician must weigh risk to benefit in these cases.


  • WARNINGS

    Patients should always be observed for at least 20 - 30 minutes after any injection. In the event of a marked systemic reaction, application of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of Epinephrine Injection (1:1,000) is recommended. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet is then gradually released at 15 minute intervals. Patients under treatment with beta-blockers may be refractory to the usual dose of epinephrine.

    Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In cases of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reaction unresponsive to the above may require cardiopulmonary resuscitation.

    DO NOT GIVE INTRAVENOUSLY

    After inserting the needle, but before injecting the dose, pull plunger of the syringe slightly. If blood returns in the syringe, discard the syringe and contents and repeat injection at another site.

    Bulk concentrated extracts must be diluted for initial therapy.

    Withhold allergenic extracts temporarily or reduce the dose in patients with any one of the following conditions:

                - Severe rhinitis or asthma symptoms;

                - Infection or flu accompanied by fever;

                - Exposure to excessive amounts of clinically relevant allergen prior to therapy.

    Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk. See PRECAUTIONS AND ADVERSE REACTIONS.

    TRANSFER OF PATIENTS

    From pyridine extracted alum complexed allergenic extracts to aqueous extracts and glycerinated: In order to avoid untoward reaction, it is recommended that therapy be initiated as though the patients were previously untreated. The first dose should be related to the patient's sensitivity, determined by history and confirmed by skin testing.

    From unstandardized aqueous extracts to standardized aqueous extracts and glycerinated: The physician should establish the potency relationship, perhaps by comparative skin testing at equal concentration, prior to injecting the first standardized dose.

    From aqueous alum precipitated or modified extracts to aqueous extracts and glycerinated: Since this subject has not been studied, it is recommended that therapy be initiated as if the patient were not previously treated.


  • PRECAUTIONS

    INFORMATION TO PATIENTS:

    Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to injection including any late reactions from previous administration. Patients should be instructed to remain in the office for 20 to 30 minutes after injection to monitor for adverse reactions. Also, see ADVERSE REACTIONS and WARNINGS Sections.

    If the protective action of allergenic extract injections is considered essential for the patient's welfare, appropriate symptomatic therapy with antihistaminic, adrenergic or other drugs might be needed either prior to or in conjunction with the allergenic extract injections.

    GENERAL:
    1. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration may be useful in unstable asthmatic to reduce the chances of exacerbation of the patient's asthma.
    2. Store allergenic extracts between 2o to 8oC at all times, even during use.
    3. Injections are to be given subcutaneously with the usual sterile precautions using a tuberculin syringe.
    4. Care must be taken to avoid injecting into a blood vessel. Pull gently on syringe plunger to determine if a blood vessel has been entered (See WARNINGS).
    5. Allergenic extracts slowly become less potent with age. During the course of treatment, it may be necessary to continue therapy with a vial of extract bearing a later expiration date. The initial dose of the extract bearing the later expiration date should be lowered to a safe, non-reaction eliciting level which can be confirmed by comparative skin testing using end-point titration.
    6. Use standard aseptic precautions when making dilutions. The first dose of the new extract should be reduced to at least 25% of the amount of the dosage from the previous extract.
    7. Extracts in 50% glycerin can cause discomfort at the site of the injection.

    PREGNANCY - CATEGORY C:      

    Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.

    Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother. However, on the basis of histamine's known ability to contract the uterine muscle, the release of significant amounts of histamine from allergen exposure or hyposensitization overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.

    PEDIATRIC USE:      

    Children can receive the same dose as adults, however, to minimize the discomfort associated with dose volume it may be advisable to reduce the volume of the dose by one-half and administer the injection at two different sites.

    NURSING MOTHERS:

    It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

    CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY:

    Studies in animals have not been performed.

    DRUG INTERACTIONS:

    Drugs can interfere with the performance of skin tests.6

          Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine), and can be as long as 40 days (astemizole).

          Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.

          Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.

          Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.

          Beta Blocking Agents: Propranolol can significantly increase skin test reactivity (See WARNINGS).

          Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.


  • ADVERSE REACTIONS

    Anaphylaxis and deaths following the injection of mite and other extracts have been reported by The British Committee on Safety in Medicine.7 Fatalities from immunotherapy in the United States since 1945 have been extensively reviewed by Lockey, R F, et al8 and more recently by Reid M J et al9.

    With careful attention to dosage and administration, such reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and OVERDOSE could result in anaphylactic symptoms. Therefore, it is imperative that physicians administering allergenic extracts understand and be prepared for the treatment of severe reactions.

    Local: Reactions at the site of injection may be immediate or delayed. Immediate wheal and erythema reactions are ordinarily of little consequence; but if very large, may be the first manifestation of a systemic reaction. If large local reactions occur, the patient should be observed for systemic symptoms for which treatment is outlined below.

    Delayed reactions start several hours after injection with local edema, erythema, itching or pain. They are usually at their peak at 24 hours and usually require no treatment. Antihistamine drugs may be administered orally.

    The next therapeutic dose should be reduced to the dose which did not elicit a reaction, and subsequent doses increased more slowly; i.e., use of intermediate dilutions.

    Systemic: Systemic reactions are characterized by one or more of the following symptoms: Sneezing, mild to severe generalized urticaria, itching other than at the injection site, extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, tachycardia, lacrimation, marked perspiration, cough, hypotension, syncope and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 to 30 minutes after any injection. Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction, unresponsive to bronchodilator, may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.2 mL to 1 mL of Epinephrine Injection (1:1,000) are recommended. Maximal recommended dose for children under 2 years of age is 0.3 mL. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet should not be left in place without loosening for 90 seconds for every 15 minutes.

    The next therapeutic injection of extract should be reduced to the dose which did not elicit a reaction, and subsequent doses increased more slowly; i.e., use of intermediate dilutions.


  • OVERDOSAGE

    Signs and symptoms of overdose are typically local and systemic reactions. For a description and management of overdose reactions, refer to "Adverse Reaction" section above.


  • DOSAGE AND ADMINISTRATION

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    When diluting bulk extracts, use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly, 10 fold dilutions are used to achieve a desired concentration for initiation and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of diluent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration.

    Starting dose for immunotherapy is related directly to a patient's sensitivity as determined by carefully executed skin testing. Degree of sensitivity can be established by determination of D5011. A general rule is to begin at 1/10 of the dose that produces sum of erythema of 50 mm (approximately a 2+ positive skin test reaction).

    For example, if a patient exhibits a 2+ intradermal reaction to 1 AU/mL, the first dose should be no higher than 0.05 mL of 0.1 AU/mL. Dosage may be increased by 0.05 mL each time until 0.5 mL is reached, at which time the next 10-fold more concentrated dilution can be used, beginning with 0.05 mL, if no untoward reaction is observed.

    Interval between doses in the early stages of immunotherapy is no more than once to twice a week, and may gradually be increased to once every two weeks. Generally, maintenance injections may be given as infrequently as once every two weeks to once a month.

    Injections are given subcutaneously, preferably in the arm. It is advantageous to give injections in alternate arms and routinely in the same area. In some patients, a local tolerance to the allergen may develop thus preventing a possible severe local reaction.

    Formal stability studies for diluted and undiluted forms of unstandardized extracts have not been performed; therefore, it is recommended that minimal amounts of the concentrate be diluted so that the diluted product is used up within a relatively short period of time; i.e., preferably not more than four weeks.

    PRE-SEASONAL METHOD OF TREATMENT

    Treatment of hay fever by the pre-seasonal method should be started 6-10 weeks prior to the usual onset of symptoms. Therapy should be started early enough to permit a graduated series of doses at 2-7 day intervals. It is recommended that the larger doses be spaced 5-7 days apart.

    Some physicians continue therapy into or through the season by repeating a reduced or MAINTENANCE dose at weekly or biweekly intervals. If during the season, hay fever symptoms develop, relief may be provided by giving supplemental treatment. If the last dose was well-tolerated and not more than 2 weeks has elapsed since it was given, this dose may be given again and repeated every 4 to 7 days.

    PERENNIAL TREATMENT

    The patient's tolerance to the offending pollen or pollens is first established by the injection of a series of graduated doses as outlined in the PRE-SEASONAL METHOD, not necessarily given pre-seasonally, since perennial therapy may be begun at any time. After completion of the ascending series of injections, from ¼ to ½ of the highest well-tolerated dose is continued at 2 to 3 week intervals throughout the year. Shortly before the usual onset of symptoms (4 to 5 weeks prior to the season), the interval between injections is shortened and the dosage is gradually increased, according to the Pre-Seasonal schedule, until maximum well-tolerated dose is again attained. This top dose should be reached just before the usual onset of symptoms at which time the treatment is discontinued. If patient's symptoms persist, therapy may be continued at a reduced dosage level, usually ¼ to ½ of the top dose.

    DOSAGE ADJUSTMENTS

    For Products Containing Short Ragweed.

    In transferring patients from unstandardized to standardized product, the physician should establish the potency relationships, perhaps by comparative skin testing, prior to injecting the first standardized dose.

    AgE is important in adjusting dosage of Short Ragweed extracts to accurately transfer a patient from older extracts to fresher material. In such cases, the dosage of AgE should be considered in addition to the W/V dilution or protein nitrogen units. Antigen E concentration continuously declines in Short Ragweed Pollen extracts at a rate that varies with the formulation of the product. Aqueous extracts retain Antigen E potency less effectively than glycerin 50% (v/v) extracts. These differences are reflected in the expiration date declared on the vial. The continuous decline should be considered. Also, where ragweed is a component of an allergen mixture, clinical response to the other components must be considered in adjustment of dosage based on AgE content alone. The usual course of immunotherapy is three to five years.

    Caution: A small percent of individuals allergic to Short Ragweed are more sensitive to minor antigens such as Ra3 Ra5 than AgE. There is no correlation between the amount of these antigens and either AgE or PNU content.

    NOTE: For extracts of Short Ragweed or equal part mixture of Short and Tall Ragweed refer to AgE dosage schedule. The AgE content for those products is indicated on the vial label. The physician may use the formula below to determine the AgE dosage for each injection.

    AgE dosage can be monitored by using the following formula:

    W/V compounded products:

    AgE dosage formula: W/V compounded products.

    PNU compounded products:

    AgE dosage formula: PNU compounded products.


  • HOW SUPPLIED

    1. Treatment Sets: 
      3 and 4 vial sets in serial dilutions prepared for therapy.
    2. Maintenance vials: 5 mL and 10 mL vials.
    3. Concentrate in multiple dose vials:
      10 mL and 50 mL, single antigens or specified mixtures, potency expressed in PNU/mL (up to and including 100,000 PNU/mL) or W/V (up to and including 1:10 W/V), aqueous or in 50% glycerin, to be diluted prior to use. 1:10 w/v short ragweed extracts contain ≥ 300 units/mL of AgE.
    4. Sterile Diluent for Allergenic Extracts (Phenol Saline) is supplied in vials of 4.5 mL, 9.0 mL, 30 mL and 100 mL.

    STORAGE:

    To maintain stability of allergenic extracts, proper storage conditions are essential. Bulk concentrates and diluted extracts are to be stored at 2o to 8o C even during use. Bulk or diluted extracts are not to be frozen. Do not use after the expiration date shown on the vial label.


  • REFERENCES

    1. Norman, P.S. et al: Immunotherapy of hayfever with ragweed antigen E. Comparisons with whole pollen extract and placebo. J. Allergy 42:93, 1968.
    2. Van Metre, T.E. et al: A controlled study of the effectiveness of the Rinkel method of immunotherapy for ragweed pollen hayfever. J. Allergy Clin.Immunol. 65:288, 1980.
    3. Umetsu, D. T. et al: Serum sickness triggered by anaphylaxis: a complication of immunotherapy. J. Allergy Clin. Immunol. 76:713, 1985.
    4. Phannphak, P. and Kohler, P. F.: Onset of polyarteritis nodosa during allergic hyposensitization treatment. Am. J. Med. 68:479, 1980.
    5. Kohler, P. F.: Immune complexes and allergic disease. In: Middleton et al: Allergy Principles and Practice 3rd Ed. St. Louis: CV Mosby, 1988:167.
    6. Bousquet, J.: In vivo methods for the study of allergy: skin test, techniques, and interpretation. In: Middleton et al: Allergy Principles and Practice 3rd Ed. St. Louis: CV Mosby, 1988:167.
    7. Committee on the Safety of Medicines. CSM update: desensitising vaccines. Brit. Med. J. 293:948, 1986.
    8. Lockey, R. F. et al: Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol. 79:660, 1987.
    9. Reid, M.J. et al: Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin. Immunol. 92:6 1993.
    10. Van Metre, T.E. et al: A controlled study of the effectiveness of the Rinkel method and the current standard method of immunotherapy for ragweed pollen hayfever. J. Allergy Clin. Immunol. 66:500, 1980.
    11. Turkeltaub, P.C., Rastogi, S.C., Baer, H., et al: A standardized quantitative skin-test assay of allergen potency and stability: studies on the allergen dose-response curve and effect of wheal, erythema, and patient selection on assay results, J. Allergy Clin. Immunol. 70:343, 1982.

    Revised June 2013

    © ALK-Abello, Inc. 2013                                                 158L

    Distributed in Canada by:
    ALK-Abelló Phamaceuticals, Inc.
    #35-151 Brunel Road
    Mississauga, Ontario
    Canada L4Z 2H6


  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel
    Allergenic Extract
    mL sterile multiple dose vial
    ALK ABELLO

    Allergenic Extract
mL sterile multiple dose vial
ALK ABELLO


  • INGREDIENTS AND APPEARANCE
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0630
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0630-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0631
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0631-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0631-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0632
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0632-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0656
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0656-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0656-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CEIBA PENTANDRA FIBER 
    kapok injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0635
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9) CEIBA PENTANDRA FIBER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0635-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0635-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUS MUSCULUS SKIN 
    mouse epithelia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0638
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0638-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0638-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUS MUSCULUS SKIN 
    mouse epithelia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0639
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0639-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ORRIS 
    iris x germanica root injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0642
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IRIS X GERMANICA ROOT (UNII: 8N6VTJ9IWV) (IRIS X GERMANICA ROOT - UNII:8N6VTJ9IWV) IRIS X GERMANICA ROOT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0642-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0642-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RABBIT 
    rabbit injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0649
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0649-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RABBIT 
    rabbit injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0650
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0650-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0650-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RABBIT 
    rabbit injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0651
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0651-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0651-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0705
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0705-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0706
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0706-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0706-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0707
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0707-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0707-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0708
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0708-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0709
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0709-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0710
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0710-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0711
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0711-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0714
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0714-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0714-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0715
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0715-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0716
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0716-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0717
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0717-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0718
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0718-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0719
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0719-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0719-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0720
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0720-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0721
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 500 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0721-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACREMONIUM STRICTUM 
    sarocladium strictum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0800
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0800-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACREMONIUM STRICTUM 
    sarocladium strictum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0801
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0801-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0801-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACREMONIUM STRICTUM 
    sarocladium strictum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0802
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0802-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACREMONIUM STRICTUM 
    sarocladium strictum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0803
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (SAROCLADIUM STRICTUM - UNII:3F36V0451W) SAROCLADIUM STRICTUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0803-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0803-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0805
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0805-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0806
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0806-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0807
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0807-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0807-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0808
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0808-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0808-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0809
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0809-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0809-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0810
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0810-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0811
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0811-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0812
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0812-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0812-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0813
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0813-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0814
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0814-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0815
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0815-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0815-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0816
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0816-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0816-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0817
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0817-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0817-30 30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3 NDC:0268-0817-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0818
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0818-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0818-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0819
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0819-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0819-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0820
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0820-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0821
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0821-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0822
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0822-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0823
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0823-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0824
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0824-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0825
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0825-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0825-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0826
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0826-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0826-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS NIGER VAR NIGER 
    aspergillus niger injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0827
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0827-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0827-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS NIGER VAR NIGER 
    aspergillus niger injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0828
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0828-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0828-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS NIGER VAR NIGER 
    aspergillus niger injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0829
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0829-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS NIGER VAR NIGER 
    aspergillus niger injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0830
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0830-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0830-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AUREOBASIDIUM PULLULANS VAR PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0832
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0832-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0832-30 30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3 NDC:0268-0832-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AUREOBASIDIUM PULLULANS VAR PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0833
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0833-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0833-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AUREOBASIDIUM PULLULANS VAR PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0834
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0834-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0834-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AUREOBASIDIUM PULLULANS VAR PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0835
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0835-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0835-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AUREOBASIDIUM PULLULANS VAR PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0836
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0836-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0836-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0837
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0837-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0837-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0838
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0838-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0839
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0839-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0840
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0840-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0840-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0841
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0841-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0842
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0842-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0843
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0843-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0843-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0844
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0844-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0844-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0845
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0845-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0845-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0846
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0846-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0847
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0847-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0848
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 0.02 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0848-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0849
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0849-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0849-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0850
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0850-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHAETOMIUM GLOBOSUM 
    chaetomium globosum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0851
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0851-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0851-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHAETOMIUM GLOBOSUM 
    chaetomium globosum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0852
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0852-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0852-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHAETOMIUM GLOBOSUM 
    chaetomium globosum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0853
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0853-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0853-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0855
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0855-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0855-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0856
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0856-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0856-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0857
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0857-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0857-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0858
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0858-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0859
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0859-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0860
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0860-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0861
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0861-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0861-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0863
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0863-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0863-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0864
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0864-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0864-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0865
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0865-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0865-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0866
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0866-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0867
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0867-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0868
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0868-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0868-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0869
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0869-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0870
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0870-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0870-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0871
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0871-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0871-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0878
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0878-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0878-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0879
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0879-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0879-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0880
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0880-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0880-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0881
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0881-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0882
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0882-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0882-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0883
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0883-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0884
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0884-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0884-30 30 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    3 NDC:0268-0884-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0885
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0885-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0885-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0886
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0886-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0886-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0887
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0887-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0888
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0888-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0889
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0889-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0890
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0890-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0891
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0891-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0892
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0892-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0892-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0893
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0893-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0894
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0894-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0894-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0895
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0895-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0895-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0896
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0896-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0896-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0897
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 1000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0897-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0898
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 10 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0898-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0899
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0899-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0899-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0900
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0900-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0901
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0901-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0901-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium vasinfectum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0902
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0902-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0902-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0903
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0903-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0904
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0904-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0905
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0905-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0906
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0906-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0911
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0911-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0911-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0912
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0912-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0912-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0913
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0913-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0913-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0914
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0914-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0914-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUCOR PLUMBEUS 
    mucor plumbeus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0915
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0915-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0915-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0916
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0916-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0916-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0917
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0917-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0917-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0918
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0918-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0919
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0919-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0919-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora intermedia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0920
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0920-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0921
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0921-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0921-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0922
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0922-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0922-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0923
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0923-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0923-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0924
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 100 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0924-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0925
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0925-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    penicillium chrysogenum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0926
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0926-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0926-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0928
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0928-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0928-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0929
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0929-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0929-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0930
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0930-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0930-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0932
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0932-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0932-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0933
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0933-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0931
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0931-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0934
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHIZOPUS ARRHIZUS VAR. ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS VAR. ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0934-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0934-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0935
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHIZOPUS ARRHIZUS VAR. ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS VAR. ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0935-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0935-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0936
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHIZOPUS ARRHIZUS VAR. ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS VAR. ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0936-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0936-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus batatas injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0937
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHIZOPUS ARRHIZUS VAR. ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS VAR. ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0937-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0937-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0939
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0939-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0939-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0940
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0940-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0941
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0941-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0942
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0942-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0943
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0943-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0943-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0944
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0944-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    USTILAGO MAYDIS 
    corn smut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0945
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0945-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0945-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    USTILAGO MAYDIS 
    corn smut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0946
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0946-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    USTILAGO TRITICI 
    loose wheat smut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0952
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0952-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0952-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0955
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0955-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0955-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0956
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0956-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0956-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0957
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0957-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0957-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0958
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 0.001 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0958-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium solani injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0959
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0959-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0959-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0961
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0961-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0961-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0962
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 40000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0962-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    2 NDC:0268-0962-50 50 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0963
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0963-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0965
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0965-05 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0966
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 20000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-0966-10 10 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-0967
    Route of Administration SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # I