Sumatriptan and Naproxen Sodium
NDC 65862-928, Sumatriptan and Naproxen Sodium, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 65862-928
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207457
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65862-928 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUMATRIPTAN SUCCINATE85 mg/1
- NAPROXEN SODIUM500 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]; Serotonin 1b Receptor Agonists [MoA]; Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65862-928-36 | 65862092836 | 9 TABLET, FILM COATED in 1 BOTTLE (65862-928-36) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f5203c66-0a40-4263-a237-b71e930e4697NADAC price for package 65862092836
GET /v1/drugs/nadac/65862092836
Use it
Look up 65862-928 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65862-928 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65862-928. 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.