NDC 0904-6363 – Divalproex Sodium

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

Human Prescription Drug 1 recall

Product NDC0904-6363

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Major Pharmaceuticals
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 (2)

Package NDCDescriptionSince
0904-6363-4580 BLISTER PACK in 1 CARTON (0904-6363-45) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKAug 11, 2013
0904-6363-61100 BLISTER PACK in 1 CARTON (0904-6363-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKAug 11, 2013

Recalls mentioning this NDC

Other Divalproex Sodium products