NDC 71335-2783 – Divalproex sodium

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

Human Prescription Drug

Product NDC71335-2783

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078853
Marketed since
June 26, 2024
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 (5)

Package NDCDescriptionSince
71335-2783-130 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-1)Oct 13, 2025
71335-2783-260 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-2)Oct 13, 2025
71335-2783-390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-3)Oct 13, 2025
71335-2783-4120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-4)Oct 13, 2025
71335-2783-5100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-5)Oct 13, 2025

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