NDC 68382-768
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
- Strength
- 200 mg
- Approval
- ANDA ANDA216167
- On the market since
- Aug 9, 2026
- Package NDCs
68382-768-0168382-768-0568382-768-0668382-768-3068382-768-78- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?