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
- 66993-082_c3c253a9-c0e5-4aa2-927e-8777ee89aa48
- Product NDC
- 66993-082
- Form
- SPRAY
- Composition / generic term
- sumatriptan
- Labeler
- Prasco Laboratories
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20200701 / 20270731
Source-listed ingredients
- SUMATRIPTAN — 20 mg/100uL
These values do not establish equivalence or a dose recommendation.
Packages
- 6 CONTAINER in 1 BOX (66993-082-69) / 100 uL in 1 CONTAINER · 66993-082-69
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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