NDC 55111-532
Divalproex sodium 125 mg capsule, delayed release
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA078979
- On the market since
- Jan 23, 2009
- Package NDCs
55111-532-0155111-532-0555111-532-3055111-532-7855111-532-79- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
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