Fenofibrate Tablet, Film Coated
Product Images NDC 43598-910

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 43598-910). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories 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

160mg500ct (160mg 500ct Ndc)

Fenofibrate Tablets USP 160 mg film-coated tablet bottle label. Contains 50 tablets for oral use. Label shows pharmacy package only, manufacturer Appco Pharma LLC, and distributor Dr. Reddy's Laboratories Inc. Includes storage instructions and a barcode.*

FDA Label Image

160mg90ct (160mg 90ct Ndc)

Fenofibrate Tablets, USP 160 mg film-coated tablets packaging label. The label indicates 90 tablets in the container, manufactured by Appco Pharma LLC and distributed by Dr. Reddy's Laboratories Inc. Storage instructions and warnings are printed, along with a barcode and the note 'NO VARNISH' on the side.*

FDA Label Image

54mg90ct (54mg 90ct Ndc)

Fenofibrate Tablets, USP 54 mg film-coated oral tablets in a bottle with a 90-tablet count, labeled by Dr. Reddy's Laboratories Inc. The label includes dosage strength, storage instructions (25°C, excursions 15-30°C), and manufacturing details from Appco Pharma LLC. The packaging also notes the product is prescription-only and instructs to see the package insert for full dosing information.*

FDA Label Image

Structure (Chemstructure1)

Chemical structure of fenofibrate, depicting its molecular arrangement including aromatic rings, ester functional groups, and chlorine substituent, as presented in the diagram.*

* 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.