Diclofenac Potassium Powder, For Solution
Product Images NDC 51672-4240

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 Potassium (NDC 51672-4240). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Diclofenac 01)

Chemical Structure (Diclofenac 01)
Chemical structure of Diclofenac Potassium showing two benzene rings with two chlorine atoms and a potassium carboxylate group attached, consistent with the active ingredient Diclofenac Potassium.*
FDA Label Image

Figure 1 (Diclofenac 02)

Figure 1 (Diclofenac 02)
A Kaplan-Meier plot depicting the percentage of subjects over time in hours. It compares Diclofenac Potassium for oral solution with placebo, showing a higher cumulative percentage of subjects for the Diclofenac Potassium group within approximately 2.25 hours.*
FDA Label Image

Principal Display Panel (50 mg Packet Carton)

Principal Display Panel (50 mg Packet Carton)
Packaging label for Diclofenac Potassium for Oral Solution USP, 50 mg powder for solution. The label includes instructions for use, warnings about phenylalanine content, storage conditions, and manufacturer information (Taro Pharmaceutical Industries Ltd. and Taro Pharmaceuticals U.S.A., Inc.). The box contains nine single-use packets and displays the NDC 51672-4240. The label features the Taro logo and highlights oral administration using water only.*

* 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.