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EPICOCCUM NIGRUM - 54575-194-50 - (epicoccum nigrum)

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Drug Information of EPICOCCUM NIGRUM

Product NDC: 54575-194
Proprietary Name: EPICOCCUM NIGRUM
Non Proprietary Name: epicoccum nigrum
Active Ingredient(s): 1    g/20mL & nbsp;   epicoccum nigrum
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of EPICOCCUM NIGRUM

Product NDC: 54575-194
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of EPICOCCUM NIGRUM

Package NDC: 54575-194-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-194-50)

NDC Information of EPICOCCUM NIGRUM

NDC Code 54575-194-50
Proprietary Name EPICOCCUM NIGRUM
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-194-50)
Product NDC 54575-194
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name epicoccum nigrum
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name EPICOCCUM NIGRUM
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE]

Complete Information of EPICOCCUM NIGRUM


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