Divalproex Sodium 250 mg (8744102701 Divalproex Sodium 250 mg)
Not available*
Divalproex Sodium Tablet, Delayed Release
Product Images NDC 87441-027
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Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 87441-027). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Unit Dose Solutions, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Divalproex Sodium 500 mg (8744102801 Divalproex Sodium 500 mg)
This is a description of Divalproex sodium tablets, USP, in 500 mg strength. It is a prescription-only medication used to treat certain conditions. The tablets are delayed-release and come with a Medication Guide to be given to each patient. The packaging meets USP standards for safety and quality. The product is distributed by Tuckahoe Enterprises, LL(, based in Henrico, VA.*
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
