Home > National Drug Code (NDC) > Clotrimazole

Clotrimazole - 51672-2062-0 - (Clotrimazole)

Alphabetical Index


Drug Information of Clotrimazole

Product NDC: 51672-2062
Proprietary Name: Clotrimazole
Non Proprietary Name: Clotrimazole
Active Ingredient(s): 2    g/100g & nbsp;   Clotrimazole
Administration Route(s): VAGINAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Clotrimazole

Product NDC: 51672-2062
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021143
Marketing Category: NDA
Start Marketing Date: 20000412

Package Information of Clotrimazole

Package NDC: 51672-2062-0
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2062-0) > 21 g in 1 TUBE, WITH APPLICATOR

NDC Information of Clotrimazole

NDC Code 51672-2062-0
Proprietary Name Clotrimazole
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2062-0) > 21 g in 1 TUBE, WITH APPLICATOR
Product NDC 51672-2062
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Clotrimazole
Dosage Form Name CREAM
Route Name VAGINAL
Start Marketing Date 20000412
Marketing Category Name NDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name CLOTRIMAZOLE
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Clotrimazole


General Information