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SUNFLOWER POLLEN - 54575-179-10 - (helianthus annuus pollen)

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Drug Information of SUNFLOWER POLLEN

Product NDC: 54575-179
Proprietary Name: SUNFLOWER POLLEN
Non Proprietary Name: helianthus annuus pollen
Active Ingredient(s): 1    g/20mL & nbsp;   helianthus annuus pollen
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SUNFLOWER POLLEN

Product NDC: 54575-179
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of SUNFLOWER POLLEN

Package NDC: 54575-179-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-179-10)

NDC Information of SUNFLOWER POLLEN

NDC Code 54575-179-10
Proprietary Name SUNFLOWER POLLEN
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-179-10)
Product NDC 54575-179
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name helianthus annuus pollen
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name HELIANTHUS ANNUUS POLLEN
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of SUNFLOWER POLLEN


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