NDC 68788-8358
Divalproex sodium 500 mg tablet, extended release
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-261.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA209286
- On the market since
- Feb 13, 2023
- Package NDCs
68788-8358-368788-8358-668788-8358-9- Official label
- DailyMed (National Library of Medicine), updated Apr 8, 2026
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