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