Drugplain

NDC 55111-530-01

divalproex sodium 250 mg/1

divalproex sodium · TABLET, DELAYED RELEASE

No Recall History

divalproex sodium is a tablet, delayed release containing divalproex sodium at a strength of 250 mg/1. Manufactured by Dr.Reddy's Laboratories Limited.

Key Facts

Brand Name
divalproex sodium
Generic Name
divalproex sodium
NDC Code (Package)
55111-530-01
NDC Code (Product)
55111-530
Manufacturer
Dr.Reddy's Laboratories Limited
Strength
250 mg/1
Dosage Form
TABLET, DELAYED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA078755
Marketing Start
07/29/2008

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.