NDC 68071-2973
Oxcarbazepine 150 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-137.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Oxcarbazepine: every company that makes it
- Form
- tablet, film coated
- Strength
- 150 mg
- Approval
- ANDA ANDA077802
- On the market since
- Oct 9, 2007
- Package NDCs
68071-2973-9- Official label
- DailyMed (National Library of Medicine), updated May 16, 2023
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