NDC 67046-1194
Divalproex Sodium 125 mg tablet, delayed release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-472.
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
- Strength
- 125 mg
- Approval
- ANDA ANDA079163
- On the market since
- Nov 12, 2024
- Package NDCs
67046-1194-3- Official label
- DailyMed (National Library of Medicine), updated Nov 12, 2024
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