Fenofibrate Tablet, Film Coated
Product Images NDC 42858-454

3 FDA label images from Rhodes Pharmaceuticals Llc · 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 Fenofibrate (NDC 42858-454). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rhodes Pharmaceuticals Llc, 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

Principal Display Panel (54 mg Tablet Bottle Label)

Principal Display Panel (54 mg Tablet Bottle Label)
Fenofibrate 54 mg film-coated tablets label for oral use by Rhodes Pharmaceuticals LLC. The label states the product is Rx only and contains 90 tablets. It includes usage instructions and safety warnings to keep the medication out of the reach of children. The label displays the NDC number and barcodes on a white and purple background with the Rhodes logo.*
FDA Label Image

Principal Display Panel (160 mg Tablet Bottle Label)

Principal Display Panel (160 mg Tablet Bottle Label)
Fenofibrate 160 mg film-coated tablets label by Rhodes Pharmaceuticals LLC. The package contains 90 tablets for oral use. The label includes dosing information, storage instructions, and safety warnings, including a notice to keep medication out of reach of children. The NDC number 42858-660-45 is visible along with a barcode.*
FDA Label Image

Chemical Structure (Structure 01)

Chemical Structure (Structure 01)
Chemical structure of fenofibrate showing the molecular composition and arrangement of atoms including chlorine, oxygen, and carbon groups, with molecular weight 360.83 and formula C20H21ClO4.*

* 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.