Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 63187-522

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 63187-522). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

78e77986-figure-01 (Diclofenac Sodium Dr Tablets Usp 1)

78e77986-figure-01 (Diclofenac Sodium Dr Tablets Usp 1)
Chemical structure of diclofenac sodium showing its molecular framework with two chlorine atoms, a carboxylate group, and an amine linkage.*
FDA Label Image

78e77986-figure-02 (Diclofenac Sodium Dr Tablets Usp 2)

78e77986-figure-02 (Diclofenac Sodium Dr Tablets Usp 2)
Diclofenac Sodium 50 mg delayed-release tablets in a white rectangular carton with purple and black text. The label displays the proprietary and generic names, dosage form, strength, and route of administration. The labeler, Proficient Rx LP, and product NDC number 63187-522 are also visible.*
FDA Label Image

63187-522-30 (Diclofenac Sodium Dr Tablets Usp 4)

63187-522-30 (Diclofenac Sodium Dr Tablets Usp 4)
Label for Diclofenac Sodium 50 mg delayed-release oral tablets by Proficient Rx LP. The label states #30 DR tablets, with instructions to dispense the Medication Guide separately. It lists the active ingredient as diclofenac sodium USP 50 mg, specifies each white, round, enteric-coated tablet is printed with a logo and the number 550 in black ink. Manufacturer is Actavis Elizabeth LLC, Elizabeth, NJ.*

* 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.