Diclofenac Potassium Capsule, Liquid Filled
Product Images NDC 59651-353

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 59651-353). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Figure1 (Diclofenac Fig1)

Figure1 (Diclofenac Fig1)
This appears to be a chart or table displaying the Mean Pain Intensity on a scale of 0-10 for different doses of 25mg Diclofenac Potassium over a period of 48 hours. It includes a legend and instructions for reading the Pain Intensity scale.*
FDA Label Image

Package Label-principal Display Panel (25 mg (120 Capsules Bottle))

Package Label-principal Display Panel (25 mg (120 Capsules Bottle))
Each liquid filled capsule contains 25mg of Diclofenac potassium USP. The capsules are distributed by Aurobindo Pharma USA, Inc. and contain a medication guide that should be provided to each patient. The capsules are manufactured in India and the usual adult dosage is one capsule four times a day or as instructed by a physician. The capsules should be stored at 20°C to 25°C and should be protected from moisture and light in a tight, light-resistant container. For complete prescribing information, refer to the package insert. The code is TS/DRUGS/16/2014 and the NDC is 59651-353-08.*
FDA Label Image

Str (Diclofenac Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.