NDC 47335-712
Topiramate 200 mg tablet, film coated
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Dadra, India | Makes it and tests it | Problems found, fixed voluntarilyMar 29, 2019 · 5 inspections |
Product details
- Generic drug
- Topiramate: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA090278
- On the market since
- Dec 15, 2014
- Package NDCs
47335-712-0847335-712-1347335-712-1847335-712-8347335-712-8647335-712-88- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2026
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