NDC 68084-782
Divalproex Sodium 500 mg tablet, delayed release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-048.
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 |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA090554
- On the market since
- Jan 26, 2016
- Package NDCs
68084-782-1168084-782-61- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2025
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