Curvularia - 49643-109-10 - (Curvularia lunata)

Alphabetical Index


Drug Information of Curvularia

Product NDC: 49643-109
Proprietary Name: Curvularia
Non Proprietary Name: Curvularia lunata
Active Ingredient(s): 1    g/10mL & nbsp;   Curvularia lunata
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Curvularia

Product NDC: 49643-109
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Curvularia

Package NDC: 49643-109-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-109-10)

NDC Information of Curvularia

NDC Code 49643-109-10
Proprietary Name Curvularia
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-109-10)
Product NDC 49643-109
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Curvularia lunata
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name COCHLIOBOLUS LUNATUS
Strength Number 1
Strength Unit g/10mL
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 Curvularia


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