Divalproex Sodium Tablet, Delayed Release
Product Images NDC 67046-0875

1 FDA label image from Coupler Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 67046-0875). 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 474 03 Divalproex Dr 500mg 67046 875 30)

Label (68001 474 03 Divalproex Dr 500mg 67046 875 30)
Label for Divalproex Sodium 500 mg delayed-release tablets by Coupler LLC. The label indicates a package of 30 tablets with identifiers including lot number, serial number, and expiration date. Storage instructions specify controlled room temperature and protection from light. The label includes barcodes and references prescribing information in an enclosure.*

* 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.