NDC 62756-798 – Divalproex Sodium

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

Human Prescription Drug 1 recall

Product NDC62756-798

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078597
Marketed since
July 29, 2008
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
62756-798-08100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-08)Jul 29, 2008
62756-798-13500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-13)Jul 29, 2008
62756-798-181000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-18)Jul 29, 2008
62756-798-8330 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-83)Jul 29, 2008
62756-798-88100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-88)Jul 29, 2008

Recalls mentioning this NDC

Other Divalproex Sodium products