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CANDIDA ALBICANS - 0268-6514-06 - (Candida albicans)

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Drug Information of CANDIDA ALBICANS

Product NDC: 0268-6514
Proprietary Name: CANDIDA ALBICANS
Non Proprietary Name: Candida albicans
Active Ingredient(s): .1    g/mL & nbsp;   Candida albicans
Administration Route(s): PERCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CANDIDA ALBICANS

Product NDC: 0268-6514
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of CANDIDA ALBICANS

Package NDC: 0268-6514-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-6514-06)

NDC Information of CANDIDA ALBICANS

NDC Code 0268-6514-06
Proprietary Name CANDIDA ALBICANS
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-6514-06)
Product NDC 0268-6514
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Candida albicans
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name CANDIDA ALBICANS
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE]

Complete Information of CANDIDA ALBICANS


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