NDC 68001-105
Divalproex Sodium 250 mg tablet, film coated, extended release
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA078239
- On the market since
- Oct 8, 2013
- Package NDCs
68001-105-0068001-105-03- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2026
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