Sumatriptan
NDC 76420-500, Sumatriptan Succinate, tablet, from Asclemed USA, Inc..
- Product NDC
- 76420-500
- Status
- Listed
- Labeler
- Asclemed USA, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078327
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76420-500 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUMATRIPTAN SUCCINATE100 mg/1
Pharmacologic classes
Serotonin 1b Receptor Agonists [MoA]; Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 76420-500-09 | 76420050009 | 9 TABLET in 1 BLISTER PACK (76420-500-09) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/77f9f135-e840-48f0-81e8-73e08433e768
Use it
Look up 76420-500 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76420-500 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76420-500. 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.