NDC product
Sulfamethoxazole and Trimethoprim
NDC 0703-9514 · Teva Parenteral Medicines, Inc.
Key facts
| Product NDC | 0703-9514 |
|---|---|
| Proprietary name | Sulfamethoxazole and Trimethoprim |
| Nonproprietary name | Sulfamethoxazole and Trimethoprim |
| Substances | SULFAMETHOXAZOLE, TRIMETHOPRIM |
| Dosage form | INJECTION, SOLUTION, CONCENTRATE |
| Route | INTRAVENOUS |
| Labeler | Teva Parenteral Medicines, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA073303 |
| Pharmacologic classes | 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] and 1 more |
| Marketing start | Nov 1, 1991 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: