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Alternaria alternata - 36987-1859-2 - (Alternaria alternata)

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Drug Information of Alternaria alternata

Product NDC: 36987-1859
Proprietary Name: Alternaria alternata
Non Proprietary Name: Alternaria alternata
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   Alternaria alternata
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Alternaria alternata

Product NDC: 36987-1859
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Alternaria alternata

Package NDC: 36987-1859-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1859-2)

NDC Information of Alternaria alternata

NDC Code 36987-1859-2
Proprietary Name Alternaria alternata
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1859-2)
Product NDC 36987-1859
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alternaria alternata
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ALTERNARIA ALTERNATA
Strength Number 20000
Strength Unit [PNU]/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 Alternaria alternata


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