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Aspergillus fumigatus - 49643-130-50 - (Aspergillus fumigatus)

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Drug Information of Aspergillus fumigatus

Product NDC: 49643-130
Proprietary Name: Aspergillus fumigatus
Non Proprietary Name: Aspergillus fumigatus
Active Ingredient(s): 1    g/10mL & nbsp;   Aspergillus fumigatus
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Aspergillus fumigatus

Product NDC: 49643-130
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Aspergillus fumigatus

Package NDC: 49643-130-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49643-130-50)

NDC Information of Aspergillus fumigatus

NDC Code 49643-130-50
Proprietary Name Aspergillus fumigatus
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49643-130-50)
Product NDC 49643-130
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Aspergillus fumigatus
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name ASPERGILLUS FUMIGATUS
Strength Number 1
Strength Unit g/10mL
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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