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SULFAMETHOXAZOLE and TRIMETHOPRIM
SULFAMETHOXAZOLE and TRIMETHOPRIM - 12634-779-04 - (SULFAMETHOXAZOLE and TRIMETHOPRIM)
Drug Information of SULFAMETHOXAZOLE and TRIMETHOPRIM
| Product NDC: | 12634-779 |
| 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: | 12634-779 |
| Labeler Name: | Apotheca, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074650 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091103 |
Package Information of SULFAMETHOXAZOLE and TRIMETHOPRIM
| Package NDC: | 12634-779-04 |
| Package Description: | 120 mL in 1 BOTTLE (12634-779-04) |
NDC Information of SULFAMETHOXAZOLE and TRIMETHOPRIM
| NDC Code | 12634-779-04 |
| Proprietary Name | SULFAMETHOXAZOLE and TRIMETHOPRIM |
| Package Description | 120 mL in 1 BOTTLE (12634-779-04) |
| Product NDC | 12634-779 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SULFAMETHOXAZOLE and TRIMETHOPRIM |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20091103 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotheca, 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] |
