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Clotrimazole and Betamethasone Dipropionate
Clotrimazole and Betamethasone Dipropionate - 51672-4048-6 - (Clotrimazole and Betamethasone Dipropionate)
Drug Information of Clotrimazole and Betamethasone Dipropionate
| Product NDC: | 51672-4048 |
| Proprietary Name: | Clotrimazole and Betamethasone Dipropionate |
| Non Proprietary Name: | Clotrimazole and Betamethasone Dipropionate |
| Active Ingredient(s): | .64; 10 mg/g; mg/g & nbsp; Clotrimazole and Betamethasone Dipropionate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clotrimazole and Betamethasone Dipropionate
| Product NDC: | 51672-4048 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075673 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010529 |
Package Information of Clotrimazole and Betamethasone Dipropionate
| Package NDC: | 51672-4048-6 |
| Package Description: | 1 TUBE in 1 CARTON (51672-4048-6) > 45 g in 1 TUBE |
NDC Information of Clotrimazole and Betamethasone Dipropionate
| NDC Code | 51672-4048-6 |
| Proprietary Name | Clotrimazole and Betamethasone Dipropionate |
| Package Description | 1 TUBE in 1 CARTON (51672-4048-6) > 45 g in 1 TUBE |
| Product NDC | 51672-4048 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clotrimazole and Betamethasone Dipropionate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20010529 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE |
| Strength Number | .64; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
