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
- 0527-1818_1fca524e-6cf5-4782-b5d5-b37b101cd93a
- Product NDC
- 0527-1818
- Form
- SPRAY
- Composition / generic term
- Sumatriptan
- Labeler
- Lannett Company, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160219
- Source listing expiry
- 20261231
Source-listed ingredients
- SUMATRIPTAN — 5 mg/.1mL
These values do not establish equivalence or a dose recommendation.
Packages
- 6 BLISTER PACK in 1 CARTON (0527-1818-43) / .1 mL in 1 BLISTER PACK · 0527-1818-43
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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