Diclofenac Potassium Capsule, Liquid Filled
Product Images NDC 71335-2550

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 71335-2550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemstructure (Chemstructure)

FDA Label Image

Figure01 (Fig01)

Figure01 (Fig01)
This text appears to be a description of a pain relief medication that includes Diclofenac Potassium as the active ingredient. It mentions a pain intensity scale with ratings from no pain to worst pain, and dosing intervals for the medication. The medication seems to be available in 25 mg doses.*
FDA Label Image

Label (Lbl713352550)

Label (Lbl713352550)
This text is a package insert for liquid-filled capsules containing 25 mg of Diclofenac Potassium, USP. The usual adult dosage is 1 capsule four times daily or as instructed by a physician. The packaging includes a QR code for complete prescribing information and a medication guide. The capsules should be stored at 20° to 25°C (68° to 77°F) in a light-resistant container and protected from moisture and light. It is important not to accept the product if the seal over the bottle opening is broken or missing and to keep it out of reach of children. The capsules are manufactured by Bryant Ranch Prepack, Inc. and repackaged by Catalent Ontario Limited.*

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