| Product NDC: | 51672-2037 |
| Proprietary Name: | Clotrimazole |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | 1 g/mL & nbsp; Clotrimazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51672-2037 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19960501 |
| Package NDC: | 51672-2037-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (51672-2037-1) > 10 mL in 1 BOTTLE |
| NDC Code | 51672-2037-1 |
| Proprietary Name | Clotrimazole |
| Package Description | 1 BOTTLE in 1 CARTON (51672-2037-1) > 10 mL in 1 BOTTLE |
| Product NDC | 51672-2037 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19960501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |