Divalproex Sodium Tablet, Delayed Release
Product Images NDC 71335-2862

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 71335-2862). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

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FDA Label Image

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FDA Label Image

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FDA Label Image

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FDA Label Image

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FDA Label Image

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FDA Label Image

Label (Lbl713352862)

Label (Lbl713352862)
The text describes an enteric-coated delayed-release tablet containing Divalproex Sodium, USP. The tablets should be stored at 20° to 25°C (68° to 77°F) and dispensed in a tight, light-resistant container as specified in the USP. It provides information from the manufacturer, Bryant Ranch Prepack, Inc, and Unichem Laboratories Ltd. Additionally, it advises to dispense the Medication Guide to each patient and to keep the package 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.