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Clotrimazole and Betamethasone Dipropionate
Clotrimazole and Betamethasone Dipropionate - 0168-0370-30 - (Clotrimazole and Betamethasone Dipropionate)
Drug Information of Clotrimazole and Betamethasone Dipropionate
| Product NDC: | 0168-0370 |
| Proprietary Name: | Clotrimazole and Betamethasone Dipropionate |
| Non Proprietary Name: | Clotrimazole and Betamethasone Dipropionate |
| Active Ingredient(s): | .5; 10 mg/mL; mg/mL & nbsp; Clotrimazole and Betamethasone Dipropionate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clotrimazole and Betamethasone Dipropionate
| Product NDC: | 0168-0370 |
| Labeler Name: | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076516 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050616 |
Package Information of Clotrimazole and Betamethasone Dipropionate
| Package NDC: | 0168-0370-30 |
| Package Description: | 30 mL in 1 BOTTLE (0168-0370-30) |
NDC Information of Clotrimazole and Betamethasone Dipropionate
| NDC Code | 0168-0370-30 |
| Proprietary Name | Clotrimazole and Betamethasone Dipropionate |
| Package Description | 30 mL in 1 BOTTLE (0168-0370-30) |
| Product NDC | 0168-0370 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clotrimazole and Betamethasone Dipropionate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20050616 |
| Marketing Category Name | ANDA |
| Labeler Name | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
| Substance Name | BETAMETHASONE; CLOTRIMAZOLE |
| Strength Number | .5; 10 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
