NDC 31722-022
Divalproex sodium 500 mg tablet, film coated, extended release
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA215527
- On the market since
- Sep 26, 2023
- Package NDCs
31722-022-0131722-022-05- Official label
- DailyMed (National Library of Medicine), updated Jul 3, 2026
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