NDC 68382-106 – Divalproex sodium

Divalproex Sodium 125 mg/1 · Capsule, Coated Pellets · Oral

Human Prescription Drug

Product NDC68382-106

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule, Coated Pellets
Route
Oral
Marketing category
ANDA · ANDA078919
Marketed since
January 27, 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 (3)

Package NDCDescriptionSince
68382-106-01100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-01)Jan 27, 2009
68382-106-101000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-10)Jan 27, 2009
68382-106-77100 BLISTER PACK in 1 CARTON (68382-106-77) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-106-30)Jan 27, 2009

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