Sumatriptan Succinate
NDC 76420-093, Sumatriptan Succinate, tablet, from Asclemed USA, Inc..
- Product NDC
- 76420-093
- Status
- Listed
- Labeler
- Asclemed USA, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076847
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76420-093 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SUMATRIPTAN SUCCINATE50 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 |
|---|---|---|
| 76420-093-09 | 76420009309 | 9 BLISTER PACK in 1 CARTON (76420-093-09) / 1 TABLET in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b16886d0-224b-4d83-85c4-bc3eb3606c17
Use it
Look up 76420-093 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76420-093 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76420-093. 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.