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Trimethoprim
Trimethoprim - 0093-2158-01 - (Trimethoprim)
Drug Information of Trimethoprim
| Product NDC: | 0093-2158 |
| Proprietary Name: | Trimethoprim |
| Non Proprietary Name: | Trimethoprim |
| Active Ingredient(s): | 100 mg/1 & nbsp; Trimethoprim |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trimethoprim
| Product NDC: | 0093-2158 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018679 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900930 |
Package Information of Trimethoprim
| Package NDC: | 0093-2158-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0093-2158-01) |
NDC Information of Trimethoprim
| NDC Code | 0093-2158-01 |
| Proprietary Name | Trimethoprim |
| Package Description | 100 TABLET in 1 BOTTLE (0093-2158-01) |
| Product NDC | 0093-2158 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trimethoprim |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | NDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | TRIMETHOPRIM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
