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Candida albicans - 36987-1915-4 - (Candida albicans)

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Drug Information of Candida albicans

Product NDC: 36987-1915
Proprietary Name: Candida albicans
Non Proprietary Name: Candida albicans
Active Ingredient(s): 40000    [PNU]/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: 36987-1915
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Candida albicans

Package NDC: 36987-1915-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1915-4)

NDC Information of Candida albicans

NDC Code 36987-1915-4
Proprietary Name Candida albicans
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1915-4)
Product NDC 36987-1915
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candida albicans
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name CANDIDA ALBICANS
Strength Number 40000
Strength Unit [PNU]/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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