Sulfamethoxazole and Trimethoprim DS is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Apotheca Inc.. The primary component is Sulfamethoxazole; Trimethoprim.
| Product ID | 12634-177_db550e63-43dc-4126-b857-010383501dd0 |
| NDC | 12634-177 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sulfamethoxazole and Trimethoprim DS |
| Generic Name | Sulfamethoxazole And Trimethoprim Ds |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1994-06-21 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076899 |
| Labeler Name | Apotheca Inc. |
| Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
| Active Ingredient Strength | 800 mg/1; mg/1 |
| Pharm Classes | Sulfonamide Antimicrobial [EPC],Sulfonamides [CS],Cytochrome P450 2C9 Inhibitors [MoA],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA],Cytochrome P450 2C8 Inhibitors [MoA],Organic Cation Transporter 2 Inhibitors [MoA] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 1994-06-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076899 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1994-06-21 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| SULFAMETHOXAZOLE | 800 mg/1 |
| SPL SET ID: | 38f42bad-6b2a-423d-af66-0e526ba03da1 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |