NDC 67046-0875
Divalproex Sodium 500 mg tablet, delayed release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-474.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unichem Laboratories Limited | Ghaziabad, India | Makes it | No problems foundFeb 13, 2024 · 7 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, 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 ANDA079163
- On the market since
- Oct 19, 2026
- Package NDCs
67046-0875-3- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?