NDC 50090-7841 – Divalproex sodium

Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC50090-7841

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA214643
Marketed since
February 25, 2022
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
50090-7841-030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-0)Dec 29, 2025
50090-7841-190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7841-1)Dec 29, 2025

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