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Candida albicans - 49288-0312-1 - (Candida albicans)

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Drug Information of Candida albicans

Product NDC: 49288-0312
Proprietary Name: Candida albicans
Non Proprietary Name: Candida albicans
Active Ingredient(s): .1    g/mL & nbsp;   Candida albicans
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Candida albicans

Product NDC: 49288-0312
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19920413

Package Information of Candida albicans

Package NDC: 49288-0312-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0312-1)

NDC Information of Candida albicans

NDC Code 49288-0312-1
Proprietary Name Candida albicans
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0312-1)
Product NDC 49288-0312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candida albicans
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19920413
Marketing Category Name BLA
Labeler Name Antigen Laboratories, 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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