Product NDC: | 51672-1260 |
Proprietary Name: | Clotrimazole |
Non Proprietary Name: | Clotrimazole |
Active Ingredient(s): | 10 mg/mL & nbsp; Clotrimazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-1260 |
Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074580 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960729 |
Package NDC: | 51672-1260-3 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (51672-1260-3) > 30 mL in 1 BOTTLE, PLASTIC |
NDC Code | 51672-1260-3 |
Proprietary Name | Clotrimazole |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (51672-1260-3) > 30 mL in 1 BOTTLE, PLASTIC |
Product NDC | 51672-1260 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clotrimazole |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19960729 |
Marketing Category Name | ANDA |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | CLOTRIMAZOLE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |