NDC 68001-474
Divalproex Sodium 500 mg tablet, delayed release
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unichem Laboratories Limited | Ghaziabad, India | Makes it | No problems foundFeb 13, 2024 · 7 inspections |
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
- Jan 20, 2021
- Package NDCs
68001-474-0068001-474-03- Official label
- DailyMed (National Library of Medicine), updated May 21, 2026
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