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Hormodendrum - 49288-0244-5 - (Hormodendrum)

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Drug Information of Hormodendrum

Product NDC: 49288-0244
Proprietary Name: Hormodendrum
Non Proprietary Name: Hormodendrum
Active Ingredient(s): .1    g/mL & nbsp;   Hormodendrum
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hormodendrum

Product NDC: 49288-0244
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Hormodendrum

Package NDC: 49288-0244-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0244-5)

NDC Information of Hormodendrum

NDC Code 49288-0244-5
Proprietary Name Hormodendrum
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0244-5)
Product NDC 49288-0244
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hormodendrum
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name CLADOSPORIUM CLADOSPORIOIDES
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Hormodendrum


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