NDC 60687-879
Divalproex Sodium 500 mg tablet, delayed release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from BluePoint Laboratories.'s NDC 68001-474.
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
- 500 mg
- Approval
- ANDA ANDA079163
- On the market since
- Feb 6, 2025
- Package NDCs
60687-879-1160687-879-61- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?