Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 71205-494

3 FDA label images from Proficient Rx Lp · 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 71205-494). 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

Figure (Dic05 0006 01)

Figure (Dic05 0006 01)
Chemical structure of Diclofenac Sodium, showing its molecular arrangement of atoms including chlorine, amino, and carboxylate groups as part of the compound's chemical formula.*
FDA Label Image

Figure (Dic05 0006 03)

Figure (Dic05 0006 03)
The image shows a white rectangular blister pack containing 10 round, light yellow tablets of Diclofenac Sodium Delayed Release, 50 mg. The pack is labeled with the proprietary name, active ingredient, strength, and dosage form. The labeler is Proficient Rx LP, and the package is intended for oral use.*
FDA Label Image

71205-494-30 (Dic05 0006 06)

71205-494-30 (Dic05 0006 06)
Label for Diclofenac Sodium Delayed Release Tablets, 50 mg strength, packaged by Proficient Rx LP. The label indicates a 30-count bottle, with dosage form as delayed-release (DR) tablets. The product is oral prescription medication distributed by Carlsbad Technology Inc. The label includes storage instructions, identification details, and multiple small labels for tablet packaging with lot and expiration placeholders.*

* 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.