NDC 67296-1420
Sumatriptan 20 mg per 0.1 mL spray
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Lannett Company, Inc.'s NDC 0527-1859.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Summit Biosciences Inc. | Lexington, KY, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 21, 2025 · 4 inspections |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- spray
- Strength
- 20 mg per 0.1 mL
- Approval
- ANDA ANDA204841
- On the market since
- Feb 19, 2016
- Package NDCs
67296-1420-2- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2024
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