United States · FDA National Drug Code directory
Sumatriptan
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 76420-500_eacf382a-98ac-e3ad-e053-2995a90a44e8
- Product NDC
- 76420-500
- Form
- TABLET
- Composition / generic term
- Sumatriptan Succinate
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090817
- Source listing expiry
- 20261231
Source-listed ingredients
- SUMATRIPTAN SUCCINATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 9 TABLET in 1 BLISTER PACK (76420-500-09) · 76420-500-09
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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