NDC 0832-7124 – Divalproex Sodium

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

Human Prescription Drug

Product NDC0832-7124

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078182
Marketed since
March 21, 2014
Marketing end
October 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0832-7124-01100 BLISTER PACK in 1 CARTON (0832-7124-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7124-89)Apr 1, 2016
0832-7124-11100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7124-11)Mar 21, 2014
0832-7124-15500 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7124-15)Mar 21, 2014

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