NDC 83270-151
sumatriptan 6 mg per 0.5 mL injection, solution
On the label: Onesource Specialty Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Onesource Specialty Pharma Limited | Bengaluru, India | Makes it, tests it, packages it, labels it and sterilizes it | Problems found, fixed voluntarilyJun 30, 2026 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Sumatriptan: 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
83270-151-07- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2026
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