NDC 70518-3055 – Divalproex Sodium

Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC70518-3055

Product details

Brand name
Divalproex Sodium
Generic name
Divalproex Sodium
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090554
Marketed since
March 23, 2021
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 (5)

Package NDCDescriptionSince
70518-3055-1100 POUCH in 1 BOX (70518-3055-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-2)Mar 16, 2022
70518-3055-3100 POUCH in 1 BOX (70518-3055-3) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-4)Aug 9, 2022
70518-3055-560 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-5)Jan 4, 2023
70518-3055-630 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-6)May 1, 2023
70518-3055-730 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3055-7)Jun 30, 2025

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