NDC 68788-7866
Oxcarbazepine 600 mg tablet, film coated
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Breckenridge Pharmaceutical, Inc.'s NDC 51991-294.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| LGM Pharma Solutions, LLC | Irvine, CA, United States | Makes it | No problems foundJan 24, 2025 · 11 inspections, 2 with FDA action |
| Towa Pharmaceutical Europe, S.L. | Martorelles, Spain | Makes it and tests it | Problems found, fixed voluntarilySep 9, 2022 · 6 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Oxcarbazepine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 600 mg
- Approval
- ANDA ANDA078069
- On the market since
- Feb 15, 2021
- Package NDCs
68788-7866-368788-7866-668788-7866-9- Official label
- DailyMed (National Library of Medicine), updated Sep 5, 2025
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