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
- 80425-0258_2a9ba8f4-6ce4-e827-e063-6394a90a0300
- Product NDC
- 80425-0258
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sumatriptan
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230117
- Source listing expiry
- 20261231
Source-listed ingredients
- SUMATRIPTAN SUCCINATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (80425-0258-1) / 9 TABLET, FILM COATED in 1 BLISTER PACK · 80425-0258-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →