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

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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 (62756 797 13 Divalproex Sodium 250mg Dr 67046 1571 30)
This is a description of Divalproex Sodium tablets in 250mg strength by Sun Pharma. The medication is enteric-coated for delayed release and should be stored at 20-25°C with excursions permitted to 15-30°C. Each tablet contains Divalproex Sodium equivalent to valproic acid. The batch number is 123456789 and it is packed by Coupler LLC in West Chester, PA. The usual dosage instructions can be found on the package insert.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.