NDC 0832-7123
Divalproex Sodium 250 mg tablet, delayed release
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA078182
- On the market since
- Mar 21, 2014
- Package NDCs
0832-7123-010832-7123-110832-7123-150832-7123-89- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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