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ASPERGILLUS FUMIGATUS - 0268-0817-10 - (ASPERGILLUS FUMIGATUS)

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Drug Information of ASPERGILLUS FUMIGATUS

Product NDC: 0268-0817
Proprietary Name: ASPERGILLUS FUMIGATUS
Non Proprietary Name: ASPERGILLUS FUMIGATUS
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   ASPERGILLUS FUMIGATUS
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ASPERGILLUS FUMIGATUS

Product NDC: 0268-0817
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of ASPERGILLUS FUMIGATUS

Package NDC: 0268-0817-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0817-10)

NDC Information of ASPERGILLUS FUMIGATUS

NDC Code 0268-0817-10
Proprietary Name ASPERGILLUS FUMIGATUS
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0817-10)
Product NDC 0268-0817
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name ASPERGILLUS FUMIGATUS
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name ASPERGILLUS FUMIGATUS
Strength Number 20000
Strength Unit [PNU]/mL
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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