NDC 68180-261
Divalproex sodium 500 mg tablet, extended release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA209286
- On the market since
- Sep 18, 2020
- Package NDCs
68180-261-0168180-261-0268180-261-06- Official label
- DailyMed (National Library of Medicine), updated May 5, 2026
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