NDC 70518-1749
divalproex sodium 125 mg capsule, coated pellets
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-106.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- capsule, coated pellets, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA078919
- On the market since
- Dec 17, 2018
- Package NDCs
70518-1749-070518-1749-1- Official label
- DailyMed (National Library of Medicine), updated Apr 30, 2026
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