NDC 72162-2460 – Divalproex Sodium

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

Human Prescription Drug

Product NDC72162-2460

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 (3)

Package NDCDescriptionSince
72162-2460-1100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1)Feb 21, 2025
72162-2460-330 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3)Feb 21, 2025
72162-2460-5500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-5)Feb 21, 2025

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