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Sulfamethoxazole and Trimethoprim
Sulfamethoxazole and Trimethoprim - 54879-007-16 - (Sulfamethoxazole and Trimethoprim)
Drug Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 54879-007 |
| Proprietary Name: | Sulfamethoxazole and Trimethoprim |
| Non Proprietary Name: | Sulfamethoxazole and Trimethoprim |
| Active Ingredient(s): | 200; 40 mg/5mL; mg/5mL & nbsp; Sulfamethoxazole and Trimethoprim |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 54879-007 |
| Labeler Name: | STI Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA018615 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19830701 |
Package Information of Sulfamethoxazole and Trimethoprim
| Package NDC: | 54879-007-16 |
| Package Description: | 473 mL in 1 BOTTLE (54879-007-16) |
NDC Information of Sulfamethoxazole and Trimethoprim
| NDC Code | 54879-007-16 |
| Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Package Description | 473 mL in 1 BOTTLE (54879-007-16) |
| Product NDC | 54879-007 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19830701 |
| Marketing Category Name | ANDA |
| Labeler Name | STI Pharma LLC |
| Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
| Strength Number | 200; 40 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA],Sulfonamide Antimicrobial [EPC],Sulfonamides [Chemical/Ingredient] |
