Product NDC: | 0591-5571 |
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) |
Product NDC: | 0591-5571 |
Labeler Name: | Watson Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070049 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100404 |
Package NDC: | 0591-5571-01 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5571-01) |
NDC Code | 0591-5571-01 |
Proprietary Name | Trimethoprim |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5571-01) |
Product NDC | 0591-5571 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Trimethoprim |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100404 |
Marketing Category Name | ANDA |
Labeler Name | Watson Laboratories, Inc. |
Substance Name | TRIMETHOPRIM |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |