NDC 50090-3416
Divalproex Sodium 250 mg tablet, delayed release
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-7123.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release
- Strength
- 250 mg
- Approval
- ANDA ANDA078182
- On the market since
- Mar 21, 2014
- Package NDCs
50090-3416-0- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2018
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