Divalproex Sodium Tablet, Delayed Release
Product Images NDC 67046-1571

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 67046-1571). 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 (62756 797 13 Divalproex Sodium 250mg Dr 67046 1571 30)

Label for Divalproex Sodium 250 mg delayed-release tablets, packaged in a quantity of 30. The label shows the product name, dosage strength, pill ID 797, and mentions it is RX only. It is labeled by Coupler LLC, with a lot number and expiration date. Storage instructions specify controlled room temperature and protection from light. Sun Pharma is also mentioned on the label.*

* 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.