Divalproex Sodium Tablet, Delayed Release
Product Images NDC 60687-879

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 60687-879). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

125 mg Divalproex Sodium Dr Tablet Blister.jpg (125 mg Divalproex Sodium Dr Tablet Blister)

125 mg Divalproex Sodium Dr Tablet Blister.jpg (125 mg Divalproex Sodium Dr Tablet Blister)
FDA Label Image

125 mg Divalproex Sodium Dr Tablets Carton.jpg (125 mg Divalproex Sodium Dr Tablets Carton)

125 mg Divalproex Sodium Dr Tablets Carton.jpg (125 mg Divalproex Sodium Dr Tablets Carton)
This text contains information about Divalproex Sodium Delayed Release Tablets, USP with 125 mg Valproic Acid Activity. The tablets are packaged in a box containing 30 tablets, to be taken as prescribed. The usual dosage and storage instructions are also provided. The product is distributed by American Health Packaging in Columbus, Ohio. The NDC number for the product is 60687-857-21.*
FDA Label Image

250 mg Divalproex Sodium Dr Tablet Blister.jpg (250 mg Divalproex Sodium Dr Tablet Blister)

250 mg Divalproex Sodium Dr Tablet Blister.jpg (250 mg Divalproex Sodium Dr Tablet Blister)
FDA Label Image

250 mg Divalproex Sodium Dr Tablets Carton.jpg (250 mg Divalproex Sodium Dr Tablets Carton)

250 mg Divalproex Sodium Dr Tablets Carton.jpg (250 mg Divalproex Sodium Dr Tablets Carton)
Description: This text provides information on Divalproex Sodium Delayed Release Tablets, USP. Each tablet contains Divalproex Sodium equivalent to Valproic acid 250mg. Usual dosage and storage instructions are included. It is advised to dispense with a medication guide to each patient. Manufacturer details are from BluPoint Laboratories distributed by American Health Packaging.*
FDA Label Image

500 mg Divalproex Sodium Dr Tablet Blister.jpg (500 mg Divalproex Sodium Dr Tablet Blister)

500 mg Divalproex Sodium Dr Tablet Blister.jpg (500 mg Divalproex Sodium Dr Tablet Blister)
FDA Label Image

500 mg Divalproex Sodium Dr Tablets Carton.jpg (500 mg Divalproex Sodium Dr Tablets Carton)

500 mg Divalproex Sodium Dr Tablets Carton.jpg (500 mg Divalproex Sodium Dr Tablets Carton)
This information pertains to Divalproex Sodium Delayed Release Tablets. Each tablet contains 500 mg of Valproic Acid. The package contains 90 tablets. The usual dosage should be as per the prescribing information. It is important to store the tablets between 20°C to 25°C. It is dispensed with a Medication Guide for patient information and safety. The product is distributed by American Health Packaging.*
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Ahp85721

Ahp85721
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Ahp86801

Ahp86801
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Ahp87961

Ahp87961
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.