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Scopulariopsis - 49288-0463-5 - (Scopulariopsis)

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Drug Information of Scopulariopsis

Product NDC: 49288-0463
Proprietary Name: Scopulariopsis
Non Proprietary Name: Scopulariopsis
Active Ingredient(s): .05    g/mL & nbsp;   Scopulariopsis
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Scopulariopsis

Product NDC: 49288-0463
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Scopulariopsis

Package NDC: 49288-0463-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49288-0463-5)

NDC Information of Scopulariopsis

NDC Code 49288-0463-5
Proprietary Name Scopulariopsis
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49288-0463-5)
Product NDC 49288-0463
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Scopulariopsis
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name MICROASCUS BREVICAULIS
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 Scopulariopsis


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