NDC 72162-2515 – Divalproex sodium

Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC72162-2515

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202419
Marketed since
June 2, 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
72162-2515-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2515-1)Jun 9, 2025

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