NDC 55111-531 – divalproex sodium

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

Human Prescription Drug

Product NDC55111-531

Product details

Brand name
divalproex sodium
Generic name
divalproex sodium
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078755
Marketed since
July 29, 2008
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Divalproex Sodium →

Package NDC codes (4)

Package NDCDescriptionSince
55111-531-01100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01)Jul 29, 2008
55111-531-05500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05)Jul 29, 2008
55111-531-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30)Jul 29, 2008
55111-531-7810 BLISTER PACK in 1 CARTON (55111-531-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)Jul 29, 2008

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