Orudis Capsule
Product Images NDC 28595-031

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Orudis (NDC 28595-031). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allegis Pharmaceuticals, 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

Chemicalstructure (63853ed1 F011 4e5a 97b9 A737394abf42)

Chemical structure diagram of ketoprofen, showing its molecular arrangement with aromatic rings and functional groups.*

FDA Label Image

Label-1 (Label 1)

Label for Orudis (ketoprofen) capsules, USP 75 mg, by Allegis Pharmaceuticals, Inc. The label includes the NDC 28595-031-60, indicates the product is prescription only, and contains 60 capsules. Instructions for storage and dispensing are provided along with a barcode and pharmacist warning to provide a medication guide to patients.*

FDA Label Image

Chart (Chart)

A data table presenting a comparison of pharmacokinetic parameters for Orudis (Ketoprofen) capsules, 4 x 50 mg. It includes metrics such as extent of oral absorption, peak plasma levels under fasted and fed conditions, time to peak concentration, area under plasma concentration-time curve (AUC), oral-dose clearance, and half-life, with values expressed as mean ± standard deviation.*

FDA Label Image

Image1 (Cee18009 1795 4bf9 9216 28b34d5dda16)

A line graph depicting the concentration (mg/L) of Orudis (Ketoprofen) over time (hours) up to 24 hours. The chart shows multiple lines indicating varied concentration profiles within the time frame, illustrating the drug's presence and decline in the bloodstream.*

* 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.