NDC 70518-2357 – Divalproex Sodium

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

Human Prescription Drug

Product NDC70518-2357

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090554
Marketed since
October 10, 2019
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 (3)

Package NDCDescriptionSince
70518-2357-030 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-0)Oct 10, 2019
70518-2357-1100 POUCH in 1 BOX (70518-2357-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2357-2)Mar 16, 2021
70518-2357-530 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-5)Aug 9, 2022

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