United States · FDA National Drug Code directory
Sumatriptan Succinate
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
- 43598-768_d0cf8002-71d2-7e4b-f04e-0120cc95dc1a
- Product NDC
- 43598-768
- Form
- INJECTION
- Composition / generic term
- Sumatriptan Succinate
- Labeler
- Dr. Reddys Laboratories Inc.,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230420
- Source listing expiry
- 20271231
Source-listed ingredients
- SUMATRIPTAN SUCCINATE — 6 mg/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 SYRINGE in 1 CARTON (43598-768-23) / .5 mL in 1 SYRINGE (43598-768-11) · 43598-768-23
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.
Browse United States records →