NDC 71335-2885 – Divalproex Sodium

Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-2885

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA079163
Marketed since
October 1, 2011
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
71335-2885-1500 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2885-1)Oct 23, 2025

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