Sulfamethox-TMP DS is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pharmpak, Inc.. The primary component is Sulfamethoxazole; Trimethoprim.
Product ID | 54348-625_8f75fb21-8080-76d4-e053-2995a90a59dd |
NDC | 54348-625 |
Product Type | Human Prescription Drug |
Proprietary Name | Sulfamethox-TMP DS |
Generic Name | Sulfamethoxazole, Trimethoprim |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2019-07-11 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076899 |
Labeler Name | PharmPak, 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 | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-07-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA076899 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-07-11 |
Marketing Category | ANDA |
Application Number | ANDA076899 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-07-11 |
Marketing Category | ANDA |
Application Number | ANDA076899 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-07-11 |
Marketing Category | ANDA |
Application Number | ANDA076899 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-07-11 |
Ingredient | Strength |
---|---|
SULFAMETHOXAZOLE | 800 mg/1 |
SPL SET ID: | ede74118-32c5-4f52-9823-509538e674c8 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |