NDC 70748-278
Topiramate 200 mg capsule, extended release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Pithampur, India | Makes it and packages it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
Product details
- Generic drug
- Topiramate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA215561
- On the market since
- Feb 3, 2026
- Package NDCs
70748-278-06- Official label
- DailyMed (National Library of Medicine), updated Mar 30, 2026
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