NDC 71335-0008 – Divalproex Sodium

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

Human Prescription Drug

Product NDC71335-0008

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 (4)

Package NDCDescriptionSince
71335-0008-130 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)Dec 21, 2018
71335-0008-260 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2)Mar 6, 2018
71335-0008-390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3)Mar 1, 2018
71335-0008-4120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4)Dec 27, 2021

Other Divalproex Sodium products