Divalproex Sodium Tablet, Delayed Release
Product Images NDC 70518-2626

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 70518-2626). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Mm2 (Divalproex Sodium 500mg 70518 2626 01)

This is a packaging label for Divalproex Sodium 500 mg delayed-release tablet, with a quantity of 1. The medication is prescription-only and should be kept out of reach of children. The label contains information about expiry date, lot number, source NDC, and manufacturer. The directions for use are included on the package insert. The medication should be stored within the temperature range of 20-26°C (63-77°F), and excursions up to 15-30°C (59-86°F) are permitted. The label was repackaged by RemedyRepack Inc. of Indiana, PA.*

FDA Label Image

Remedy_label (Remedy Label)

Divalproex Sodium is a delayed-release tablet of 500 mg, packaged in 100 quantity. It is RX only and has an NDC number of 70518-2626-00. The lot number and expiry date are not available. It is sourced from Unichem Pharma Inc, NJ. Proper storage conditions are indicated on the package insert, and Repackaged by RemedyRepack Inc, Indiana. The medication should be kept out of the reach of children.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.