NDC 71335-2344 – Divalproex Sodium

Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-2344

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078597
Marketed since
July 29, 2008
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 (5)

Package NDCDescriptionSince
71335-2344-160 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-1)May 30, 2024
71335-2344-230 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-2)May 30, 2024
71335-2344-390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-3)Jan 29, 2024
71335-2344-4180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-4)May 30, 2024
71335-2344-5120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-5)May 30, 2024

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