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Aspergillus repens - 36987-1875-2 - (Aspergillus repens)

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Drug Information of Aspergillus repens

Product NDC: 36987-1875
Proprietary Name: Aspergillus repens
Non Proprietary Name: Aspergillus repens
Active Ingredient(s): 10000    [PNU]/mL & nbsp;   Aspergillus repens
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aspergillus repens

Product NDC: 36987-1875
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Aspergillus repens

Package NDC: 36987-1875-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (36987-1875-2)

NDC Information of Aspergillus repens

NDC Code 36987-1875-2
Proprietary Name Aspergillus repens
Package Description 10 mL in 1 VIAL, MULTI-DOSE (36987-1875-2)
Product NDC 36987-1875
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Aspergillus repens
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name EUROTIUM HERBARIORUM
Strength Number 10000
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 Aspergillus repens


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