Diclofenac Potassium Powder, For Solution
Product Images NDC 69315-506

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diclofenac Potassium (NDC 69315-506). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leading Pharma, 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.

FDA Label Image

Chemical Structure (Cambia Figure 1)

Chemical structure of diclofenac potassium, a nonsteroidal anti-inflammatory drug, showing a biphenyl nucleus with two chlorine atoms, an amine linkage, and a potassium carboxylate group.*

FDA Label Image

Graph (Cambia Figure 2)

A line graph comparing the percent of subjects over time in hours between two groups labeled "CAMBIA" and "Placebo." The y-axis shows percent of subjects from 0 to 30, and the x-axis shows time ranging from 0.00 to about 2.25 hours. The solid line represents CAMBIA, and the dotted line represents Placebo, with CAMBIA showing a higher percent of subjects over the time course.*

FDA Label Image

Cartonlabel (Cartonlabel)

Packaging label for DICLOFENAC POTASSIUM 50 mg powder for oral solution by Leading Pharma, LLC. The label includes dosing instructions to mix the powder in water only, the product is prescription only, and the package contains nine total packets. Distributed by Leading Pharma, manufactured under license from APR Applied Pharma Research SA.*

FDA Label Image

Sachetlabel (Sachetlabel)

This image shows the Drug Facts label for Diclofenac Potassium 50 mg Powder for Oral Solution by Leading Pharma. It includes directions on how to open individual dose packets, dosage information advising storage at 25°C with permitted excursions, safety warning to keep out of reach of children, and manufacturer/distributor details including Leading Pharma, LLC and APR Applied Pharma Research SA, Switzerland.*

* 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.