Fenofibrate Tablet
Product Images NDC 71335-2628

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 71335-2628). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Image (020746a2 302e 4d60 B8e6 Bfa0e9a96838 01)

Chemical structure of fenofibrate, the active ingredient in FENOFIBRATE tablets. The diagram depicts the molecular arrangement of atoms and bonds specific to fenofibrate.*

FDA Label Image

Label (Lbl713352628)

Fenofibrate Tablets USP 40 mg label showing 90 tablets in the bottle. The label includes NDC 71335-2628-1 and highlights the 40 mg strength. It is relabeled by Bryant Ranch Prepack and manufactured by V-Ensure Pharma Technologies Pvt. Ltd. Storage and safety instructions are also present on the label.*

FDA Label Image

Label 2 (Lbl713352629)

Fenofibrate Tablets USP 120 mg label displaying the National Drug Code (NDC) 71335-2629-1. The label indicates 90 tablets per container and the product is for oral use with prescription only. It shows the labeler as Bryant Ranch Prepack and the manufacturer as V-Ensure Pharma Technologies Pvt. Ltd. Storage instructions and child safety warnings are included.*

* 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.