Divalproex Sodium Capsule, Coated Pellets
Product Images NDC 55154-4759

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 55154-4759). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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

FDA Label Image

Figure 1

Figure 1
This is a chart or graph displaying the percentage reduction in CPS (probably a medical or neurological condition) rate for patients taking Divalproex Sodium delayed-release tablets versus a placebo. The chart shows that 50% of the patients taking the medication had improvement, while some had no change and others experienced worsening. There is no additional information to provide a clearer context.*
FDA Label Image

Figure 2

Figure 2
FDA Label Image

Guide

Guide
This text provides instructions on how to open and handle a large capsule containing coated particles to prevent spillage. The user should hold the capsule carefully and twist it gently to separate the top from the bottom. The sprinkles inside the capsule should be added to a small amount of soft food and swallowed immediately without chewing. Drinking water afterward is recommended. Unused sprinkle and food mixture should be thrown away, and the mixture should be prepared each time before it is taken.*
FDA Label Image

Structure

Structure
FDA Label Image

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This is a package of Divalproex Sodium 125mg delayed-release capsules which are used to treat certain types of seizures and manic episodes in people with bipolar disorder. The package contains 10 capsules which can be swallowed or opened and mixed with food. It is advised to go through the product insert for complete instructions and warnings. The package should be stored at a controlled room temperature between 20°C to 25°C, and away from the reach of children. It is not safe for child use and should be dispensed only for institutional use. The manufacturer is American Health Packaging and it is distributed by Cardinal Health. NDC number of the drug product is 68382-106.*

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