Dr.reddy's Laboratories Limited
Visakhapatnam, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection May 17, 2024. 9 inspections on record, 2 with serious problems.
NDC 43598-768
Sumatriptan Succinate 6 mg per 0.5 mL injection
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
Product details
- Generic drug
- Sumatriptan: see every company that makes it
- Form
- injection, subcutaneous
- Strength
- 6 mg per 0.5 mL
- Approval
- ANDA ANDA090495
- On the market since
- Apr 20, 2023
- Package NDCs
43598-768-1143598-768-23- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2026
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