NDC 67046-1683 – divalproex sodium

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

Human Prescription Drug

Product NDC67046-1683

Product details

Brand name
divalproex sodium
Generic name
divalproex sodium
Labeler
Coupler LLC
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078853
Marketed since
July 6, 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
67046-1683-330 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1683-3)Jul 6, 2026

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