NDC 68071-2717
Divalproex Sodium 250 mg tablet, delayed release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-047.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release
- Strength
- 250 mg
- Approval
- ANDA ANDA090554
- On the market since
- Oct 24, 2014
- Package NDCs
68071-2717-6- Official label
- DailyMed (National Library of Medicine), updated May 20, 2022
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