Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 80425-0197

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 80425-0197). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of 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.

Product Images & Figures Index

FDA Label Image

Description (Description)

Description (Description)
Chemical structure of Diclofenac Sodium, showing two chlorinated aromatic rings connected by an amine linkage with a carboxylate functional group indicating the sodium salt form.*
FDA Label Image

Lab 1 (Label 1)

Lab 1 (Label 1)
The label is for Diclofenac Sodium 50 mg delayed-release tablets. It includes the product name and strength prominently in green text. The label shows it is packed by Advanced Rx Pharmacy of Tennessee, LLC, located in Nashville, TN. It also displays storage instructions (20°-25°C), a barcode, lot number, expiration date (4/30/2025), and NDC numbers for comparison and source.*
FDA Label Image

Lab 2 (Label 2)

Lab 2 (Label 2)
Packaging label for Diclofenac Sodium 50 mg delayed-release tablets from Advanced Rx Pharmacy of Tennessee, LLC. The label includes the proprietary name Diclofenac Sodium DR, strength 50 mg, dosage form as a delayed-release tablet, and indicates the product is for oral use. It also shows storage instructions and barcodes for product identification.*

* 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.