Product NDC: | 13551-501 |
Proprietary Name: | Primsol |
Non Proprietary Name: | trimethoprim hydrochloride |
Active Ingredient(s): | 50 mg/5mL & nbsp; trimethoprim hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13551-501 |
Labeler Name: | FSC Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA074973 |
Marketing Category: | NDA |
Start Marketing Date: | 20000124 |
Package NDC: | 13551-501-01 |
Package Description: | 20 mL in 1 BOTTLE, PLASTIC (13551-501-01) |
NDC Code | 13551-501-01 |
Proprietary Name | Primsol |
Package Description | 20 mL in 1 BOTTLE, PLASTIC (13551-501-01) |
Product NDC | 13551-501 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | trimethoprim hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20000124 |
Marketing Category Name | NDA |
Labeler Name | FSC Laboratories, Inc |
Substance Name | TRIMETHOPRIM HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |