NDC 82804-233 – divalproex sodium

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

Human Prescription Drug

Product NDC82804-233

Product details

Brand name
divalproex sodium
Generic name
divalproex sodium
Labeler
Proficient Rx LP
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078853
Marketed since
June 26, 2024
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 (1)

Package NDCDescriptionSince
82804-233-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)Aug 6, 2025

Other Divalproex Sodium products