NDC 68180-265
Divalproex Sodium 125 mg tablet, delayed release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA078790
- On the market since
- Jul 29, 2008
- Package NDCs
68180-265-0168180-265-0268180-265-11- Official label
- DailyMed (National Library of Medicine), updated May 5, 2026
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