NDC 55111-532 – Divalproex sodium

Divalproex Sodium 125 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC55111-532

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Dr. Reddy's Laboratories Ltd
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078979
Marketed since
January 23, 2009
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 (4)

Package NDCDescriptionSince
55111-532-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-01)Jan 23, 2009
55111-532-05500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-05)Jan 23, 2009
55111-532-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-30)Jan 23, 2009
55111-532-7810 BLISTER PACK in 1 CARTON (55111-532-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-532-79)Jan 23, 2009

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