Diclofenac Potassium Powder, For Solution
Product Images NDC 13668-672

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Diclofenac Potassium (NDC 13668-672). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Torrent Pharmaceuticals Limited, 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

Image Description (Carton)

Image Description (Carton)
Label for Diclofenac Potassium for Oral Solution, USP 50 mg powder for solution by Torrent Pharmaceuticals Limited. The label states pharmacist instructions, packet contents, and directions for use, including dilution with water. It also includes storage conditions, manufacturer details, NDC 13668-672-64, and a barcode. The package contains nine packets.*
FDA Label Image

Structure (Chemical Structure)

Structure (Chemical Structure)
Chemical structure of diclofenac potassium, showing two aromatic rings with chlorine substitutions and a carboxylate potassium salt group.*
FDA Label Image

Figure1 (Figure 1)

Figure1 (Figure 1)
A line graph displaying the percent of subjects over time in hours comparing Diclofenac Potassium and Placebo. The x-axis represents time in hours up to 2.25, and the y-axis represents percent of subjects up to 30%. Two lines indicate responses for Diclofenac Potassium and Placebo groups, showing differing trends over time.*
FDA Label Image
FDA Label Image
FDA Label Image

Sachet (Sachet)

Sachet (Sachet)
The image shows a strip of four labels for Diclofenac Potassium for Oral Solution, USP 50 mg. Each label includes the proprietary name, strength, dosage form, and directions for opening the packet. The labels display the NDC 13668-672-11, the Torrent Pharmaceuticals Limited logo, and indicate Rx only status.*

* 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.