NDC 60687-857
Divalproex Sodium 125 mg tablet, delayed release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from BluePoint Laboratories.'s NDC 68001-472.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unichem Laboratories Limited | Ghaziabad, India | Makes it | No problems foundFeb 13, 2024 · 7 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, delayed release, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA079163
- On the market since
- Mar 17, 2025
- Package NDCs
60687-857-1160687-857-21- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2025
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