Divalproex Sodium Tablet, Delayed Release
Product Images NDC 29300-140

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 29300-140). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unichem Pharmaceuticals (usa), 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

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This is a description of a bottle of delayed-release Depakote tablets. It contains 100 tablets of a drug called Valproic Acid. The bottle should be stored between 20°C and 25°C. The prescription information is enclosed in the package. The tablets are made by a company called Unichem Laboratories in India and are sold in the USA by Unichem Pharmaceuticals. The National Drug Code (NDC) for these tablets is 29300-139-01.*

FDA Label Image

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This is a medication label for Diyalproex Sodium tablets manufactured by Unichem Pharmaceuticals. Each tablet is enteric-coated and contains valproic acid. The tablets are delayed-release and should be stored at room temperature. The label includes information for pharmacists to dispense the medication with an enclosed medication guide to each patient. The container should not be accepted if the seal is broken or missing. The enclosed prescribing information includes Valproic Acid Activity. Only 100 tablets are included in the bottle.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.