Structural Formula (Divalproexertablet Figure 01)
Divalproex Sodium Tablet, Film Coated, Extended Release
Product Images NDC 68001-106
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 68001-106). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Bluepoint Laboratories, 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
Figure 1 (Divalproexertablet Figure 02)
Figure 2 (Divalproexertablet Figure 03)
This document appears to be a chart or graph showing the percentage reduction in CPS rate for two different doses of delayed-release divalproex sodium tablets. The chart shows that at a high dose, there is a 50% improvement rate, while at a low dose, there is no change or worsening. There is no further context or explanation provided.*
Figure 3 (Divalproexertablet Figure 04)
Divalproex Sodium Er Tablets 250mg 100tablets Rev 04-17 (Image 01)
Once-Daily Dosing extended-release tablets of Divalproex Sodium in 250mg strength are available in a pack of 10 tablets with the NDC code 68001-105-00 Rx Only. The tablets are used to treat various medical conditions but their specific use is not mentioned. Storage instructions advise to keep them at the temperature of 27°C to 25°C and in dry conditions. The validity of the medication should be checked before use. The text also contains some unclear characters that could not be evaluated in any particular language.*
Divalproex Sodium Er Tablets 500mg 100tablets Rev 04-17 (Image 02)
* 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.
