NDC 50090-4737
Divalproex sodium 500 mg tablet, film coated, extended release
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Aurobindo Pharma Limited's NDC 65862-595.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA202419
- On the market since
- Jun 2, 2014
- Package NDCs
50090-4737-050090-4737-1- Official label
- DailyMed (National Library of Medicine), updated Mar 18, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?