NDC 0074-7327 – Depakote

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

Human Prescription Drug

Product NDC0074-7327

Product details

Brand name
Depakote
Generic name
Divalproex Sodium
Labeler
AbbVie Inc.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
NDA · NDA018723
Marketed since
March 10, 1983
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Depakote →

Package NDC codes (1)

Package NDCDescriptionSince
0074-7327-13100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-7327-13)Mar 10, 1983

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