Sulfamethoxazole and Trimethoprim
NDC 71335-0762, Sulfamethoxazole and Trimethoprim, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-0762
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090624
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0762 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFAMETHOXAZOLE800 mg/1
- TRIMETHOPRIM160 mg/1
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]; Sulfonamides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-0762-0 | 71335076200 | 21 TABLET in 1 BOTTLE (71335-0762-0) |
| 71335-0762-1 | 71335076201 | 20 TABLET in 1 BOTTLE (71335-0762-1) |
| 71335-0762-2 | 71335076202 | 14 TABLET in 1 BOTTLE (71335-0762-2) |
| 71335-0762-3 | 71335076203 | 10 TABLET in 1 BOTTLE (71335-0762-3) |
| 71335-0762-4 | 71335076204 | 28 TABLET in 1 BOTTLE (71335-0762-4) |
| 71335-0762-5 | 71335076205 | 40 TABLET in 1 BOTTLE (71335-0762-5) |
| 71335-0762-6 | 71335076206 | 6 TABLET in 1 BOTTLE (71335-0762-6) |
| 71335-0762-7 | 71335076207 | 60 TABLET in 1 BOTTLE (71335-0762-7) |
| 71335-0762-8 | 71335076208 | 30 TABLET in 1 BOTTLE (71335-0762-8) |
| 71335-0762-9 | 71335076209 | 13 TABLET in 1 BOTTLE (71335-0762-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/27bebe39-c069-4a9d-99d1-c7cf44ac2f41
Use it
Look up 71335-0762 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0762 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0762. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.