United States · FDA National Drug Code directory
Tosymra
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
- 70792-812_803144a8-2d17-47ac-98d0-515198ba722d
- Product NDC
- 70792-812
- Form
- SPRAY
- Composition / generic term
- Sumatriptan
- Labeler
- Tonix Medicines, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20230701
- Source listing expiry
- 20261231
Source-listed ingredients
- SUMATRIPTAN — 10 mg/.1mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (70792-812-59) / 1 BOTTLE, SPRAY in 1 BLISTER PACK / .1 mL in 1 BOTTLE, SPRAY · 70792-812-59
- 6 BLISTER PACK in 1 CARTON (70792-812-61) / 1 BOTTLE, SPRAY in 1 BLISTER PACK / .1 mL in 1 BOTTLE, SPRAY · 70792-812-61
- 1 BLISTER PACK in 1 CARTON (70792-812-89) / 1 BOTTLE, SPRAY in 1 BLISTER PACK / .1 mL in 1 BOTTLE, SPRAY · 70792-812-89
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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