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ASPERGILLUS GLAUCUS - 54575-183-02 - (eurotium herbariorum)

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Drug Information of ASPERGILLUS GLAUCUS

Product NDC: 54575-183
Proprietary Name: ASPERGILLUS GLAUCUS
Non Proprietary Name: eurotium herbariorum
Active Ingredient(s): 1    g/20mL & nbsp;   eurotium herbariorum
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ASPERGILLUS GLAUCUS

Product NDC: 54575-183
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of ASPERGILLUS GLAUCUS

Package NDC: 54575-183-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-183-02)

NDC Information of ASPERGILLUS GLAUCUS

NDC Code 54575-183-02
Proprietary Name ASPERGILLUS GLAUCUS
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-183-02)
Product NDC 54575-183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name eurotium herbariorum
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name EUROTIUM HERBARIORUM
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 ASPERGILLUS GLAUCUS


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