Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 68071-5319

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 68071-5319). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals, Inc., 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

Jpg (68071 5319 1)

Packaging label for Diclofenac Sodium 50 mg delayed release oral tablets by NuCare Pharmaceuticals, Inc. The label shows the product name and strength, dosage form as tablets, and indicates prescription use only (Rx Only). It includes the NDC number 68071-5319-1 and mentions the labeler as NuCare Pharmaceuticals, Inc. The label also provides cautionary storage instructions and a warning to keep out of reach of children.*

FDA Label Image

Chemical Structure (Diclofenac Str)

Chemical structure of diclofenac sodium, illustrating its molecular arrangement including benzene rings, chlorine atoms, amine group, and carboxylate sodium salt functional group.*

* 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.