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CHAETOMIUM GLOBOSUM - 54575-191-50 - (chaetomium globosum)

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Drug Information of CHAETOMIUM GLOBOSUM

Product NDC: 54575-191
Proprietary Name: CHAETOMIUM GLOBOSUM
Non Proprietary Name: chaetomium globosum
Active Ingredient(s): 1    g/20mL & nbsp;   chaetomium globosum
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CHAETOMIUM GLOBOSUM

Product NDC: 54575-191
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of CHAETOMIUM GLOBOSUM

Package NDC: 54575-191-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (54575-191-50)

NDC Information of CHAETOMIUM GLOBOSUM

NDC Code 54575-191-50
Proprietary Name CHAETOMIUM GLOBOSUM
Package Description 50 mL in 1 VIAL, MULTI-DOSE (54575-191-50)
Product NDC 54575-191
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name chaetomium globosum
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name CHAETOMIUM GLOBOSUM
Strength Number 1
Strength Unit g/20mL
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 CHAETOMIUM GLOBOSUM


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