NDC 70518-3683
Divalproex Sodium 125 mg tablet, delayed release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-106.
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
- 125 mg
- Approval
- ANDA ANDA090554
- On the market since
- Mar 17, 2023
- Package NDCs
70518-3683-070518-3683-170518-3683-2- Official label
- DailyMed (National Library of Medicine), updated Jun 4, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?