NDC 67046-141
Divalproex Sodium 250 mg tablet, delayed release
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-047.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Coupler Enterprises, Location not on file · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release
- Strength
- 250 mg
- Approval
- ANDA ANDA090554
- On the market since
- Sep 28, 2017
- Package NDCs
67046-141-0767046-141-1467046-141-1567046-141-2067046-141-2167046-141-2867046-141-3067046-141-60- Official label
- DailyMed (National Library of Medicine), updated Sep 28, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?