NDC 65862-402 – Divalproex Sodium

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

Human Prescription Drug

Product NDC65862-402

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 (5)

Package NDCDescriptionSince
65862-402-01100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-01)Oct 24, 2014
65862-402-05500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-05)Oct 24, 2014
65862-402-1010 BLISTER PACK in 1 CARTON (65862-402-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACKOct 24, 2014
65862-402-393000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-39)Oct 24, 2014
65862-402-991000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-99)Oct 24, 2014

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