NDC 71610-030 – Divalproex Sodium

Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71610-030

Product details

Brand name
Divalproex Sodium
Generic name
divalproex sodium
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077567
Marketed since
January 29, 2009
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 (5)

Package NDCDescriptionSince
71610-030-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-30)Nov 12, 2018
71610-030-6090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-60)Jan 18, 2018
71610-030-75150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-75)Feb 9, 2018
71610-030-80180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-80)Jul 10, 2019
71610-030-92270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-92)Jul 10, 2019

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