NDC 67046-1137
Divalproex Sodium 250 mg tablet, film coated, extended release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-105.
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
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 250 mg
- Approval
- ANDA ANDA078239
- On the market since
- Nov 8, 2024
- Package NDCs
67046-1137-3- Official label
- DailyMed (National Library of Medicine), updated Nov 8, 2024
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