NDC 63187-742 – Divalproex Sodium

Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC63187-742

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Proficient Rx LP
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA079163
Marketed since
October 1, 2011
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 (3)

Package NDCDescriptionSince
63187-742-3030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30)Oct 3, 2016
63187-742-6060 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)Oct 3, 2016
63187-742-9090 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90)Oct 3, 2016

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