NDC 68084-415
Divalproex Sodium 500 mg tablet, film coated, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from BluePoint Laboratories.'s NDC 68001-106.
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 |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA078239
- On the market since
- Nov 21, 2013
- Package NDCs
68084-415-0168084-415-0268084-415-1168084-415-93- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2025
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