Mucor - 49643-114-30 - (Mucor racemosus)

Alphabetical Index


Drug Information of Mucor

Product NDC: 49643-114
Proprietary Name: Mucor
Non Proprietary Name: Mucor racemosus
Active Ingredient(s): 1    g/10mL & nbsp;   Mucor racemosus
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mucor

Product NDC: 49643-114
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Mucor

Package NDC: 49643-114-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (49643-114-30)

NDC Information of Mucor

NDC Code 49643-114-30
Proprietary Name Mucor
Package Description 30 mL in 1 VIAL, MULTI-DOSE (49643-114-30)
Product NDC 49643-114
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Mucor racemosus
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name MUCOR RACEMOSUS
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 Mucor


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