NDC 57237-048
Divalproex Sodium 500 mg tablet, delayed release
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA090554
- On the market since
- Oct 24, 2014
- Package NDCs
57237-048-0157237-048-05- Official label
- DailyMed (National Library of Medicine), updated May 19, 2026
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