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Sulfamethoxazole and Trimethoprim
Sulfamethoxazole and Trimethoprim - 0703-9503-03 - (sulfamethoxazole and trimethoprim)
Drug Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 0703-9503 |
| Proprietary Name: | Sulfamethoxazole and Trimethoprim |
| Non Proprietary Name: | sulfamethoxazole and trimethoprim |
| Active Ingredient(s): | 80; 16 mg/mL; mg/mL & nbsp; sulfamethoxazole and trimethoprim |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 0703-9503 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073303 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19911101 |
Package Information of Sulfamethoxazole and Trimethoprim
| Package NDC: | 0703-9503-03 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-9503-03) > 5 mL in 1 VIAL, SINGLE-DOSE (0703-9503-01) |
NDC Information of Sulfamethoxazole and Trimethoprim
| NDC Code | 0703-9503-03 |
| Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-9503-03) > 5 mL in 1 VIAL, SINGLE-DOSE (0703-9503-01) |
| Product NDC | 0703-9503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfamethoxazole and trimethoprim |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19911101 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
| Strength Number | 80; 16 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antimicrobial [EPC],Sulfonamides [Chemical/Ingredient],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
