NDC Code | 57237-232-01 |
Package Description | 100 TABLET in 1 BOTTLE (57237-232-01) |
Product NDC | 57237-232 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Sulfamethoxazole And Trimethoprim |
Non-Proprietary Name | Sulfamethoxazole And Trimethoprim |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20100216 |
Marketing Category Name | ANDA |
Application Number | ANDA090624 |
Manufacturer | Rising Pharma Holdings, Inc. |
Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
Strength | 400; 80 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Dihydrofolate Reductase Inhibitor Antibacterial [EPC], Dihydrofolate Reductase Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], Sulfonamide Antimicrobial [EPC], Sulfonamides [CS] |