Fenofibrate Tablet
Product Images NDC 72162-2469

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 Fenofibrate (NDC 72162-2469). 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)

Image (020746a2 302e 4d60 B8e6 Bfa0e9a96838 01)
Chemical structure of fenofibrate, showing its molecular configuration with chlorine, aromatic rings, and ester functional groups as part of the fenofibrate active ingredient molecule.*
FDA Label Image

2469 (Lbl721622469)

2469 (Lbl721622469)
Label for Fenofibrate Tablets, USP 40 mg, oral tablet, containing 90 tablets. Label shows NDC 72162-2469-9 and indicates the product is relabeled by Bryant Ranch Prepack, Inc. and manufactured by V-Ensure Pharma Technologies Pvt. Ltd. Storage instructions and warnings about child-resistant packaging and keeping out of reach of children are included.*
FDA Label Image

Label (Lbl721622470)

Label (Lbl721622470)
Label for Fenofibrate Tablets, USP 120 mg, oral tablets in a package of 90 tablets. The product is relabeled by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by V-Ensure Pharma Technologies Pvt. Ltd. The label includes storage instructions, a barcode, and QR codes for the package insert and additional prescribing information.*

* 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.