NDC 70518-0041
Sumatriptan 50 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-147.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- tablet
- Strength
- 50 mg
- Approval
- ANDA ANDA078327
- On the market since
- Jun 6, 2016
- Package NDCs
70518-0041-070518-0041-1- Official label
- DailyMed (National Library of Medicine), updated Aug 11, 2025
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