Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 71610-068

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 71610-068). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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.

FDA Label Image

Bottle Label 50 mg (71610 0068 80)

Label for Diclofenac Sodium DR 50 mg delayed release tablets. The package contains 180 oral tablets. Manufactured by Actavis Elizabeth LLC, Elizabeth, NJ, and repackaged by Aphena Pharma Solutions - Tennessee, LLC in Cookeville, TN. The label includes storage instructions and states the product is prescription only.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

1 (Image 1)

Chemical structure of Diclofenac Sodium showing its molecular configuration including two chlorine atoms, a carboxylate group with sodium ion, and aromatic rings.*

FDA Label Image

1 (Image 2)

Diclofenac Sodium 50 mg delayed-release tablets in a white and gray blister pack. Each tablet is round, white, and marked with '71610 068' on one side and scored on the other. The packaging shows the labeler as Aphena Pharma Solutions - Tennessee, LLC.*

FDA Label Image

1 (Image 3)

Packaging label for Diclofenac Sodium 50 mg delayed-release tablets. The carton features the product name, dosage strength, and form. It includes the labeler name, Aphena Pharma Solutions - Tennessee, LLC, and displays the package configuration and National Drug Code (NDC) 71610-068.*

* 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.