NDC 50090-7121 – Divalproex Sodium

Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC50090-7121

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
A-S Medication Solutions
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090554
Marketed since
October 24, 2014
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Divalproex Sodium →

Package NDC codes (1)

Package NDCDescriptionSince
50090-7121-030 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7121-0)Mar 27, 2024

Other Divalproex Sodium products