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Nigrospora sphaerica - 36987-2023-3 - (Nigrospora sphaerica)

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Drug Information of Nigrospora sphaerica

Product NDC: 36987-2023
Proprietary Name: Nigrospora sphaerica
Non Proprietary Name: Nigrospora sphaerica
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Nigrospora sphaerica
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nigrospora sphaerica

Product NDC: 36987-2023
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Nigrospora sphaerica

Package NDC: 36987-2023-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-2023-3)

NDC Information of Nigrospora sphaerica

NDC Code 36987-2023-3
Proprietary Name Nigrospora sphaerica
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-2023-3)
Product NDC 36987-2023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nigrospora sphaerica
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name KHUSKIA ORYZAE
Strength Number 40000
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 Nigrospora sphaerica


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