Candida - 49693-1101-1 - (Candida parapsilosis)

Alphabetical Index


Drug Information of Candida

Product NDC: 49693-1101
Proprietary Name: Candida
Non Proprietary Name: Candida parapsilosis
Active Ingredient(s): 4    [hp_X]/10mL & nbsp;   Candida parapsilosis
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Candida

Product NDC: 49693-1101
Labeler Name: USPharmaCo
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20091215

Package Information of Candida

Package NDC: 49693-1101-1
Package Description: 1 BOTTLE in 1 BOX (49693-1101-1) > 10 mL in 1 BOTTLE

NDC Information of Candida

NDC Code 49693-1101-1
Proprietary Name Candida
Package Description 1 BOTTLE in 1 BOX (49693-1101-1) > 10 mL in 1 BOTTLE
Product NDC 49693-1101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Candida parapsilosis
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20091215
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name USPharmaCo
Substance Name CANDIDA PARAPSILOSIS
Strength Number 4
Strength Unit [hp_X]/10mL
Pharmaceutical Classes

Complete Information of Candida


General Information