NDC 68001-647-00
divalproex sodium 500 mg/1
divalproex sodium · TABLET, FILM COATED, EXTENDED RELEASE
divalproex sodium is a tablet, film coated, extended release containing divalproex sodium at a strength of 500 mg/1. Manufactured by BluePoint Laboratories.
Key Facts
- Brand Name
- divalproex sodium
- Generic Name
- divalproex sodium
- NDC Code (Package)
68001-647-00- NDC Code (Product)
68001-647- Manufacturer
- BluePoint Laboratories
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA214643
- Marketing Start
- 06/06/2025
Recall History
No Recall HistoryView Full Drug Page
divalproex sodium — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.