NDC 60687-915
divalproex sodium 500 mg tablet, film coated, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from BluePoint Laboratories.'s NDC 68001-647.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unichem Laboratories Limited | Bardez, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJul 15, 2024 · 6 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA214643
- On the market since
- Dec 29, 2025
- Package NDCs
60687-915-0160687-915-0260687-915-1160687-915-93- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2026
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