Divalproex Sodium Tablet, Delayed Release
Product Images NDC 67046-1683

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 67046-1683). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coupler Llc, 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

Label (69452 434 30 Divalproex Dr 250mg 67046 1683 30)

Label for divalproex sodium delayed-release tablets, 250 mg strength. The label indicates a count of 30 tablets and includes storage instructions, manufacturer Coupler LLC, and barcode information. It states each tablet contains divalproex sodium equivalent to 250 mg valproic acid, with directions to see enclosed prescribing information. The label notes it is for prescription use only.*

* 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.