Ketoprofen
Product Images NDC 67296-0369

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 Ketoprofen (NDC 67296-0369). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug 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

Ketoprofen Structural Formula (2934cfc0 14ca 4081 964f C85c65a7f03f 01)

Ketoprofen Structural Formula (2934cfc0 14ca 4081 964f C85c65a7f03f 01)
Chemical structure of ketoprofen, showing the molecular arrangement of benzene rings, carbonyl group, and propanoic acid side chain with a methyl substitution.*
FDA Label Image

Ketoprofen Plasma Concentrations In Subjects Receiving Ketoprofen Capsules 50 mg Every 4 Hours For 16 Hours (2934cfc0 14ca 4081 964f C85c65a7f03f 02)

Ketoprofen Plasma Concentrations In Subjects Receiving Ketoprofen Capsules 50 mg Every 4 Hours For 16 Hours (2934cfc0 14ca 4081 964f C85c65a7f03f 02)
A line graph depicting concentration (mg/L) versus time (hours) over a 24-hour period. Multiple lines show varying concentration profiles with shaded areas indicating variation or confidence intervals around the lines.*
FDA Label Image

Copy Of Label (67296 3195 05)

Copy Of Label (67296 3195 05)
Label for Ketoprofen 75 mg capsules, containing 30 capsules per container. The label indicates prescription use only, with storage instructions at controlled room temperature (20-25°C). Manufactured by Teva Pharmaceuticals USA, Sellersville, PA, and distributed by Redpharm Drug, Eden Prairie, MN. The NDC is 67296-0369-2.*

* 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.