NDC Code | 70518-4217-0 |
Package Description | 1 TUBE in 1 CARTON (70518-4217-0) / 45 g in 1 TUBE |
Product NDC | 70518-4217 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Clotrimazole And Betamethasone Dipropionate |
Non-Proprietary Name | Clotrimazole And Betamethasone Dipropionate |
Dosage Form | CREAM |
Usage | TOPICAL |
Start Marketing Date | 20241021 |
Marketing Category Name | ANDA |
Application Number | ANDA075673 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE |
Strength | .5; 10 |
Strength Unit | mg/g; mg/g |
Pharmacy Classes | Azole Antifungal [EPC], Azoles [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |