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
- 80425-0318_20ae108a-00c6-a984-e063-6394a90aaaae
- Product NDC
- 80425-0318
- Form
- TABLET
- Composition / generic term
- Sumatriptan
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230407
- Source listing expiry
- 20261231
Source-listed ingredients
- SUMATRIPTAN SUCCINATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (80425-0318-1) / 9 TABLET in 1 BLISTER PACK · 80425-0318-1
- 4 BLISTER PACK in 1 CARTON (80425-0318-2) / 9 TABLET in 1 BLISTER PACK · 80425-0318-2
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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