United States · FDA National Drug Code directory
sumatriptan succinate
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
- 62756-522_55125fc1-837d-05ea-e063-6394a90a57ca
- Product NDC
- 62756-522
- Form
- TABLET, FILM COATED
- Composition / generic term
- sumatriptan succinate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090810
- Source listing expiry
- 20271231
Source-listed ingredients
- SUMATRIPTAN SUCCINATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (62756-522-01) / 9 TABLET, FILM COATED in 1 BLISTER PACK · 62756-522-01
- 100 TABLET, FILM COATED in 1 BOTTLE (62756-522-08) · 62756-522-08
- 1000 TABLET, FILM COATED in 1 BOTTLE (62756-522-18) · 62756-522-18
- 30 TABLET, FILM COATED in 1 BOTTLE (62756-522-83) · 62756-522-83
- 9 BLISTER PACK in 1 CARTON (62756-522-93) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 62756-522-93
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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