Candida - 57520-0283-1 - (Candida albicans)

Alphabetical Index


Drug Information of Candida

Product NDC: 57520-0283
Proprietary Name: Candida
Non Proprietary Name: Candida albicans
Active Ingredient(s): 200    [hp_C]/mL & nbsp;   Candida albicans
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Candida

Product NDC: 57520-0283
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100408

Package Information of Candida

Package NDC: 57520-0283-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0283-1)

NDC Information of Candida

NDC Code 57520-0283-1
Proprietary Name Candida
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0283-1)
Product NDC 57520-0283
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Candida albicans
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100408
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name CANDIDA ALBICANS
Strength Number 200
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of Candida


General Information