NDC 0904-6615 – Divalproex sodium

Divalproex Sodium 125 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC0904-6615

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Major Pharmaceuticals
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078979
Marketed since
January 23, 2009
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 (1)

Package NDCDescriptionSince
0904-6615-61100 BLISTER PACK in 1 CARTON (0904-6615-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACKJan 23, 2009

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