NDC 70518-2391
Topiramate 200 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Cipla USA., Inc.'s NDC 69097-125.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cipla Limited | Pune, India | Makes it | Problems found, fixed voluntarilyMay 8, 2024 · 7 inspections |
| Cipla Limited | Bengaluru, India | Makes the active ingredient and tests it | Problems found, fixed voluntarilyNov 13, 2024 · 7 inspections |
Product details
- Generic drug
- Topiramate: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA076343
- On the market since
- Oct 28, 2019
- Package NDCs
70518-2391-070518-2391-170518-2391-270518-2391-3- Official label
- DailyMed (National Library of Medicine), updated Jul 9, 2026
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