NDC 68071-3525
Sumatriptan 50 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Bionpharma Inc.'s NDC 69452-345.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| OrBion Pharmaceuticals Private Limited | Kancheepuram, India | Makes it, tests it, packages it and labels it | No problems foundOct 27, 2025 · 6 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA078284
- On the market since
- Feb 18, 2022
- Package NDCs
68071-3525-9- Official label
- DailyMed (National Library of Medicine), updated Feb 3, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?