Fenofibrate Tablet
Product Images NDC 72789-410

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 72789-410). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789410 Label (72789410)

72789410 Label (72789410)
Label for Fenofibrate USP 160 mg oral tablets by PD-Rx Pharmaceuticals, Inc. The label indicates a package of 30 tablets with NDC 72789-410-30. It shows dosage strength, manufacturer details including Oklahoma City, OK address, and safety warning to keep out of reach of children. The lot number is F24A71 with an expiration date of 05/2026.*
FDA Label Image

1 (Fenofibrate Tablets Usp 54 mg And 160 mg 1)

1 (Fenofibrate Tablets Usp 54 mg And 160 mg 1)
Chemical structure diagram of fenofibrate, showing its molecular framework with characteristic chlorine, aromatic rings, and ester functional groups as typically seen in fenofibrate's molecular structure.*

* 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.