NDC 65862-403 – Divalproex Sodium

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

Human Prescription Drug

Product NDC65862-403

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090554
Marketed since
October 24, 2014
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
65862-403-01100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-01)Oct 24, 2014
65862-403-05500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-05)Oct 24, 2014
65862-403-1010 BLISTER PACK in 1 CARTON (65862-403-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACKOct 24, 2014
65862-403-222000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-22)Oct 24, 2014

Other Divalproex Sodium products