Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 80425-0569

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 80425-0569). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx 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.

FDA Label Image

Diclofenac Sodium Dr 50mg #60 (Diclofenac Sodium Dr 50mg 80425 0569 01)

Diclofenac Sodium Dr 50mg #60 (Diclofenac Sodium Dr 50mg 80425 0569 01)
Label for Diclofenac Sodium Delayed Release 50 mg oral tablets, bottle of 60, from Advanced Rx of Tennessee, LLC. The label includes NDC 80425-0569-01, comparison to Voltaren XR, storage instructions between 20° and 25°C, expiration date 12/31/2027, and barcode markings.*
FDA Label Image

Diclofenac Sodium Dr 50mg #90 (Diclofenac Sodium Dr 50mg 80425 0569 02)

Diclofenac Sodium Dr 50mg #90 (Diclofenac Sodium Dr 50mg 80425 0569 02)
Label for Diclofenac Sodium Delayed Release 50 mg tablets, bottle count 90. The label displays comparison to Voltaren XR and includes NDC 80425-0569-02. It is manufactured by Advanced Rx of Tennessee, LLC, located in Nashville, TN. The label shows storage instructions and has multiple barcodes and tracking information.*
FDA Label Image

Figure (Dic05 0006 01)

Figure (Dic05 0006 01)
Chemical structure of Diclofenac Sodium, showing two chlorinated aromatic rings connected by an amine group with a carboxylate substituent.*

* 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.