NDC 70518-2370
Oxcarbazepine 300 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Breckenridge Pharmaceutical, Inc.'s NDC 51991-293.
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 |
Product details
- Generic drug
- Oxcarbazepine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA078069
- On the market since
- Oct 19, 2019
- Package NDCs
70518-2370-070518-2370-170518-2370-270518-2370-3- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2026
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