Nigrospora - 49288-0328-3 - (Nigrospora)

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Drug Information of Nigrospora

Product NDC: 49288-0328
Proprietary Name: Nigrospora
Non Proprietary Name: Nigrospora
Active Ingredient(s): .05    g/mL & nbsp;   Nigrospora
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nigrospora

Product NDC: 49288-0328
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Nigrospora

Package NDC: 49288-0328-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49288-0328-3)

NDC Information of Nigrospora

NDC Code 49288-0328-3
Proprietary Name Nigrospora
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49288-0328-3)
Product NDC 49288-0328
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nigrospora
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name KHUSKIA ORYZAE
Strength Number .05
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 Nigrospora


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