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Aspergillus flavus - 36987-1870-4 - (Aspergillus flavus)

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Drug Information of Aspergillus flavus

Product NDC: 36987-1870
Proprietary Name: Aspergillus flavus
Non Proprietary Name: Aspergillus flavus
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Aspergillus flavus
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aspergillus flavus

Product NDC: 36987-1870
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 flavus

Package NDC: 36987-1870-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1870-4)

NDC Information of Aspergillus flavus

NDC Code 36987-1870-4
Proprietary Name Aspergillus flavus
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1870-4)
Product NDC 36987-1870
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Aspergillus flavus
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ASPERGILLUS FLAVUS
Strength Number 40000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Aspergillus flavus


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