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Trichophyton schoenleinii - 49288-0618-1 - (Trichophyton schoenleinii)

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Drug Information of Trichophyton schoenleinii

Product NDC: 49288-0618
Proprietary Name: Trichophyton schoenleinii
Non Proprietary Name: Trichophyton schoenleinii
Active Ingredient(s): .05    g/mL & nbsp;   Trichophyton schoenleinii
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Trichophyton schoenleinii

Product NDC: 49288-0618
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Trichophyton schoenleinii

Package NDC: 49288-0618-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0618-1)

NDC Information of Trichophyton schoenleinii

NDC Code 49288-0618-1
Proprietary Name Trichophyton schoenleinii
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0618-1)
Product NDC 49288-0618
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trichophyton schoenleinii
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name TRICHOPHYTON SCHOENLEINII
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 Trichophyton schoenleinii


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