NDC 53808-0358
Divalproex Sodium 500 mg tablet, delayed release
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-267.
Where the pills inside were 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
- Strength
- 500 mg
- Approval
- ANDA ANDA078790
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0358-1- Official label
- DailyMed (National Library of Medicine), updated May 24, 2010
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