Drugplain

NDC 46708-821-10

Divalproex sodium 125 mg/1

Divalproex sodium · CAPSULE, DELAYED RELEASE

No Recall History

Divalproex sodium is a capsule, delayed release containing divalproex sodium at a strength of 125 mg/1. Manufactured by Alembic Pharmaceuticals Limited.

Key Facts

Brand Name
Divalproex sodium
Generic Name
Divalproex sodium
NDC Code (Package)
46708-821-10
NDC Code (Product)
46708-821
Manufacturer
Alembic Pharmaceuticals Limited
Strength
125 mg/1
Dosage Form
CAPSULE, DELAYED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA218793
Marketing Start
12/23/2024

Recall History

No Recall History

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