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
63187-323_0cdfb1de-15e5-4697-b443-ec4c7db9d432
Product NDC
63187-323
Form
TABLET
Composition / generic term
SUMATRIPTAN
Labeler
Proficient Rx LP
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

  • 1 BLISTER PACK in 1 CARTON (63187-323-09) / 9 TABLET in 1 BLISTER PACK · 63187-323-09

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.

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