Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 80425-0102

3 FDA label images from Advanced Rx Of Tennessee, Llc · 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 80425-0102). 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.

Product Images & Figures Index

FDA Label Image

Diclofenac Sodium 50mg Tab Qty 60 Ndc 80425 0102

Diclofenac Sodium 50mg Tab Qty 60 Ndc 80425 0102
Label for Diclofenac Sodium 50 mg delayed release tablets, bottle of 60, labeled by Advanced Rx of Tennessee, LLC. The label shows the product name, strength, form, quantity, and NDC 80425-0102, along with lot number, expiration date, and storage conditions. It includes a barcode and a caution about drug transfer restrictions.*
FDA Label Image

Diclofenac Sodium 50mg Tab Qty 90 Ndc 80425 0102

Diclofenac Sodium 50mg Tab Qty 90 Ndc 80425 0102
Diclofenac Sodium 50 mg delayed release tablets, bottle label showing count of 90 tablets. The label indicates advanced Rx of Tennessee, LLC as the packer located in Nashville, TN. Includes NDC 80425-0102-03, lot number, expiration date, and a federal transfer warning. Compares product to Voltaren XR. Storage instructions specify temperature 20°-25°C (68°-77°F).*
FDA Label Image

Structure

Structure
Chemical structure of diclofenac sodium showing two benzene rings with chlorine atoms and a sodium carboxylate group, representing the active ingredient diclofenac sodium.*

* 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.