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Sulfamethoxazole and Trimethoprim
Sulfamethoxazole and Trimethoprim - 50383-824-21 - (Sulfamethoxazole and Trimethoprim)
Drug Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 50383-824 |
| 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: | 50383-824 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074650 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19971229 |
Package Information of Sulfamethoxazole and Trimethoprim
| Package NDC: | 50383-824-21 |
| Package Description: | 4 TRAY in 1 CASE (50383-824-21) > 10 CUP, UNIT-DOSE in 1 TRAY > 20 mL in 1 CUP, UNIT-DOSE (50383-824-20) |
NDC Information of Sulfamethoxazole and Trimethoprim
| NDC Code | 50383-824-21 |
| Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Package Description | 4 TRAY in 1 CASE (50383-824-21) > 10 CUP, UNIT-DOSE in 1 TRAY > 20 mL in 1 CUP, UNIT-DOSE (50383-824-20) |
| Product NDC | 50383-824 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19971229 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
| Strength Number | 200; 40 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Sulfonamide Antimicrobial [EPC],Sulfonamides [Chemical/Ingredient],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
