NDC 70518-3055
Divalproex Sodium 250 mg tablet, delayed release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-047.
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
- 250 mg
- Approval
- ANDA ANDA090554
- On the market since
- Mar 23, 2021
- Package NDCs
70518-3055-070518-3055-170518-3055-270518-3055-370518-3055-470518-3055-570518-3055-670518-3055-7- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
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