NDC 70518-3477
Divalproex sodium 500 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
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
- Aug 16, 2022
- Package NDCs
70518-3477-070518-3477-170518-3477-270518-3477-370518-3477-470518-3477-570518-3477-6- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2026
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