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Divalproex Sodium Tablet, Delayed Release
Product Images NDC 51655-365
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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 51655-365). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Northwind Health Company, 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.
Product Images & Figures Index
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UWNICHEM PHARMACEUTICALS (USA). INC. is a pharmaceutical company based in the United States.*
Label (51655 365 52 Master Bottle Label Approval Rev A 05 20)
This is a bottle of Divalproex Sodium Delayed Release tablets. Each tablet contains 250 mg of valproex sodium, equivalent to valproic acid. The bottle contains 30 tablets and should be stored at controlled room temperature between 20-25°C (68-77°F). The packaging includes a warning to keep out of reach of children. The tablets are made by Unichem Pharmaceuticals and were repackaged by Northwind Pharmaceuticals in Indianapolis. The lot number is 0000000000 and the expiration is 00/00/0000. Dosage instructions should be found in the package insert.*
* 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.
