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
- 63304-099_9bc4f2da-41f0-42e2-98b2-b689c02d0a3e
- Product NDC
- 63304-099
- Form
- TABLET
- Composition / generic term
- Sumatriptan
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090210
- Source listing expiry
- 20261231
Source-listed ingredients
- SUMATRIPTAN SUCCINATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (63304-099-13) · 63304-099-13
- 1 BLISTER PACK in 1 CARTON (63304-099-19) / 9 TABLET in 1 BLISTER PACK · 63304-099-19
- 5 TABLET in 1 BOTTLE (63304-099-45) · 63304-099-45
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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