NDC 55111-533 – Divalproex Sodium

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

Human Prescription Drug 2 recalls

Product NDC55111-533

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Dr. Reddy's Laboratories Ltd
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090161
Marketed since
August 11, 2013
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 (5)

Package NDCDescriptionSince
55111-533-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-533-01)Aug 11, 2013
55111-533-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-533-05)Aug 11, 2013
55111-533-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-533-30)Aug 11, 2013
55111-533-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-533-60)Aug 11, 2013
55111-533-7810 BLISTER PACK in 1 CARTON (55111-533-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-533-79)Aug 11, 2013

Recalls mentioning this NDC

Other Divalproex Sodium products