NDC 70518-4575 – Divalproex Sodium

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

Human Prescription Drug

Product NDC70518-4575

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA079163
Marketed since
February 17, 2026
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 (1)

Package NDCDescriptionSince
70518-4575-030 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-4575-0)Feb 17, 2026

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