NDC 71610-031 – Divalproex Sodium

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

Human Prescription Drug

Product NDC71610-031

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078182
Marketed since
March 21, 2014
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
71610-031-6090 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-031-60)Jan 19, 2018

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