NDC 70518-2357
Divalproex Sodium 500 mg tablet, delayed release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-048.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA090554
- On the market since
- Oct 10, 2019
- Package NDCs
70518-2357-070518-2357-170518-2357-270518-2357-370518-2357-470518-2357-5- Official label
- DailyMed (National Library of Medicine), updated Jul 23, 2026
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