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ASPERGILLUS FUMIGATUS - 54575-182-30 - (aspergillus fumigatus)

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Drug Information of ASPERGILLUS FUMIGATUS

Product NDC: 54575-182
Proprietary Name: ASPERGILLUS FUMIGATUS
Non Proprietary Name: aspergillus fumigatus
Active Ingredient(s): 1    g/20mL & nbsp;   aspergillus fumigatus
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ASPERGILLUS FUMIGATUS

Product NDC: 54575-182
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 FUMIGATUS

Package NDC: 54575-182-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (54575-182-30)

NDC Information of ASPERGILLUS FUMIGATUS

NDC Code 54575-182-30
Proprietary Name ASPERGILLUS FUMIGATUS
Package Description 30 mL in 1 VIAL, MULTI-DOSE (54575-182-30)
Product NDC 54575-182
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name aspergillus fumigatus
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name ASPERGILLUS FUMIGATUS
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of ASPERGILLUS FUMIGATUS


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