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
- 45802-598_d1aeb8e8-e726-405a-bf9d-7436af66c48b
- Product NDC
- 45802-598
- Form
- SPRAY
- Composition / generic term
- sumatriptan
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201004
- Source listing expiry
- 20271231
Source-listed ingredients
- SUMATRIPTAN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 CONTAINER in 1 CARTON (45802-598-06) / 1 SPRAY in 1 CONTAINER (45802-598-00) · 45802-598-06
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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