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NDC 68788-7345-04 SULFATRIM 200; 40 mg/5mL; mg/5mL Details
SULFATRIM 200; 40 mg/5mL; mg/5mL
SULFATRIM is a ORAL SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is SULFAMETHOXAZOLE; TRIMETHOPRIM.
MedlinePlus Drug Summary
Co-trimoxazole is used to treat certain bacterial infections, such as pneumonia (a lung infection), bronchitis (infection of the tubes leading to the lungs), and infections of the urinary tract, ears, and intestines. It also is used to treat 'travelers' diarrhea. Co-trimoxazole is a combination of trimethoprim and sulfamethoxazole and is in a class of medications called sulfonamides. It works by stopping the growth of bacteria. Antibiotics will not kill viruses that can cause colds, flu, or other viral infections.
Related Packages: 68788-7345-04Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Co-trimoxazole
Product Information
| NDC | 68788-7345 |
|---|---|
| Product ID | 68788-7345_a702383c-a960-4cac-bf40-5d14b0ddbd98 |
| Associated GPIs | 16990002301810 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | SULFATRIM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Sulfamethoxazole and Trimethoprim |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SUSPENSION |
| Route | ORAL |
| Active Ingredient Strength | 200; 40 |
| Active Ingredient Units | mg/5mL; mg/5mL |
| Substance Name | SULFAMETHOXAZOLE; TRIMETHOPRIM |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Pharmaceutical Class | Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Dihydrofolate Reductase Inhibitor Antibacterial [EPC], Dihydrofolate Reductase Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], Sulfonamide Antimicrobial [EPC], Su |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA018615 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-7345-04 (68788734504)
| NDC Package Code | 68788-7345-4 |
|---|---|
| Billing NDC | 68788734504 |
| Package | 473 mL in 1 BOTTLE (68788-7345-4) |
| Marketing Start Date | 2020-06-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |