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Grass Smut Mixture - 49288-0214-4 - (Grass Smut Mixture)

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Drug Information of Grass Smut Mixture

Product NDC: 49288-0214
Proprietary Name: Grass Smut Mixture
Non Proprietary Name: Grass Smut Mixture
Active Ingredient(s): .05; .05    g/mL; g/mL & nbsp;   Grass Smut Mixture
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Grass Smut Mixture

Product NDC: 49288-0214
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Grass Smut Mixture

Package NDC: 49288-0214-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49288-0214-4)

NDC Information of Grass Smut Mixture

NDC Code 49288-0214-4
Proprietary Name Grass Smut Mixture
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49288-0214-4)
Product NDC 49288-0214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Grass Smut Mixture
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name SPORISORIUM CRUENTUM; USTILAGO CYNODONTIS
Strength Number .05; .05
Strength Unit g/mL; 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],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 Grass Smut Mixture


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