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Sulfamethoxazole and Trimethoprim
Sulfamethoxazole and Trimethoprim - 51079-128-20 - (Sulfamethoxazole and Trimethoprim)
Drug Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 51079-128 |
| Proprietary Name: | Sulfamethoxazole and Trimethoprim |
| Non Proprietary Name: | Sulfamethoxazole and Trimethoprim |
| Active Ingredient(s): | 800; 160 mg/1; mg/1 & nbsp; Sulfamethoxazole and Trimethoprim |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfamethoxazole and Trimethoprim
| Product NDC: | 51079-128 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071017 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110818 |
Package Information of Sulfamethoxazole and Trimethoprim
| Package NDC: | 51079-128-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-128-20) > 1 TABLET in 1 BLISTER PACK (51079-128-01) |
NDC Information of Sulfamethoxazole and Trimethoprim
| NDC Code | 51079-128-20 |
| Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-128-20) > 1 TABLET in 1 BLISTER PACK (51079-128-01) |
| Product NDC | 51079-128 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110818 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
| Strength Number | 800; 160 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Sulfonamide Antimicrobial [EPC],Sulfonamides [Chemical/Ingredient],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
