Corn Smut - 36987-2149-4 - (Corn Smut)

Alphabetical Index


Drug Information of Corn Smut

Product NDC: 36987-2149
Proprietary Name: Corn Smut
Non Proprietary Name: Corn Smut
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   Corn Smut
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Corn Smut

Product NDC: 36987-2149
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Corn Smut

Package NDC: 36987-2149-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2149-4)

NDC Information of Corn Smut

NDC Code 36987-2149-4
Proprietary Name Corn Smut
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2149-4)
Product NDC 36987-2149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Corn Smut
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name USTILAGO MAYDIS
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 Corn Smut


General Information