Onesource Specialty Pharma Limited
Bengaluru, India · makes it, tests it, packages it, labels it and sterilizes it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 9 inspections on record, 1 with serious problems.
NDC 83270-152
sumatriptan 6 mg per 0.5 mL injection, solution
On the label: Onesource Specialty Pharma Limited.
Where it's made
Product details
- Generic drug
- Sumatriptan: see every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 6 mg per 0.5 mL
- Approval
- ANDA ANDA090314
- On the market since
- Feb 2, 2026
- Package NDCs
83270-152-07- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2026
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