NDC 70518-2036 – Divalproex Sodium

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

Human Prescription Drug

Product NDC70518-2036

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203730
Marketed since
April 24, 2019
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
70518-2036-0100 POUCH in 1 BOX (70518-2036-0) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2036-1)Apr 24, 2019

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