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Trichophyton mentagrophytes - 36987-2135-4 - (Trichophyton mentagrophytes)

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Drug Information of Trichophyton mentagrophytes

Product NDC: 36987-2135
Proprietary Name: Trichophyton mentagrophytes
Non Proprietary Name: Trichophyton mentagrophytes
Active Ingredient(s): .1    g/mL & nbsp;   Trichophyton mentagrophytes
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Trichophyton mentagrophytes

Product NDC: 36987-2135
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Trichophyton mentagrophytes

Package NDC: 36987-2135-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-2135-4)

NDC Information of Trichophyton mentagrophytes

NDC Code 36987-2135-4
Proprietary Name Trichophyton mentagrophytes
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-2135-4)
Product NDC 36987-2135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trichophyton mentagrophytes
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name TRICHOPHYTON MENTAGROPHYTES
Strength Number .1
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 Trichophyton mentagrophytes


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