Divalproex Sodium Tablet, Film Coated, Extended Release
Product Images NDC 67046-1631

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 67046-1631). 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 (68001 647 03 Divalproex Er 500mg 67046 1631 30)

Label for divalproex sodium 500 mg extended-release film-coated tablets by Coupler LLC. The label shows quantity of 30 tablets with US prescription only status. Storage instructions indicate controlled room temperature and protection from light. Includes barcodes, lot number, expiration date June 23, 2026, and packaging address in West Chester, PA.*

* 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.