Candida - 49643-105-50 - (Candida albicans)

Alphabetical Index


Drug Information of Candida

Product NDC: 49643-105
Proprietary Name: Candida
Non Proprietary Name: Candida albicans
Active Ingredient(s): 1    g/20mL & nbsp;   Candida albicans
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Candida

Product NDC: 49643-105
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of Candida

Package NDC: 49643-105-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (49643-105-50)

NDC Information of Candida

NDC Code 49643-105-50
Proprietary Name Candida
Package Description 50 mL in 1 VIAL, MULTI-DOSE (49643-105-50)
Product NDC 49643-105
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name Candida albicans
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name CANDIDA ALBICANS
Strength Number 1
Strength Unit g/20mL
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


General Information