NDC 70518-4575
Divalproex Sodium 500 mg tablet, delayed release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
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 17, 2026
- Package NDCs
70518-4575-0- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2026
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