NDC 87441-027
Divalproex Sodium 250 mg tablet, delayed release
On the label: Unit Dose Solutions, Inc.. It's repackaged: Unit Dose Solutions, Inc. rebottles it from BluePoint Laboratories.'s NDC 68001-473.
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
- Unit Dose Solutions, Inc., Raleigh, NC, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA079163
- On the market since
- Jun 17, 2026
- Package NDCs
87441-027-01- Official label
- DailyMed (National Library of Medicine), updated Jun 17, 2026
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