NDC 68382-358
Topiramate 200 mg capsule, extended release
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Topiramate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA207382
- On the market since
- Nov 13, 2023
- Package NDCs
68382-358-0168382-358-0568382-358-0668382-358-3068382-358-78- Official label
- DailyMed (National Library of Medicine), updated Mar 30, 2026
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