NDC 71610-249 – Divalproex sodium

Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71610-249

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 · ANDA202419
Marketed since
June 2, 2014
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 (6)

Package NDCDescriptionSince
71610-249-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-30)Sep 15, 2020
71610-249-5360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-53)Mar 14, 2019
71610-249-6090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-60)Mar 14, 2019
71610-249-70120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-70)Mar 14, 2019
71610-249-74500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-74)Jun 12, 2026
71610-249-80180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-80)Oct 9, 2020

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