NDC 0904-7182 – Divalproex Sodium

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

Human Prescription Drug

Product NDC0904-7182

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203730
Marketed since
June 1, 2015
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
0904-7182-4580 BLISTER PACK in 1 CARTON (0904-7182-45) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 1, 2015
0904-7182-61100 BLISTER PACK in 1 CARTON (0904-7182-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 1, 2015

Other Divalproex Sodium products