NDC 51991-294
Oxcarbazepine 600 mg tablet, film coated
On the label: Breckenridge Pharmaceutical, Inc..
Where it's 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
- 600 mg
- Approval
- ANDA ANDA078069
- On the market since
- Jan 11, 2008
- Package NDCs
51991-294-0151991-294-05- Official label
- DailyMed (National Library of Medicine), updated Jan 9, 2024
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