NDC 62756-299
phenytoin sodium 200 mg capsule, extended release
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Product details
- Generic drug
- Phenytoin: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040731
- On the market since
- Jun 30, 2008
- Package NDCs
62756-299-0862756-299-1362756-299-8362756-299-88- Official label
- DailyMed (National Library of Medicine), updated Dec 14, 2022
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