Fenofibrate Tablet
Product Images NDC 0115-5522

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 0115-5522). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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.

Product Images & Figures Index

FDA Label Image

Fenofibrate-tablet-1 (Fenofibrate Tablets 54 mg And 160 mg 0115 1)

Fenofibrate-tablet-1 (Fenofibrate Tablets 54 mg And 160 mg 0115 1)
Chemical structure of fenofibrate, showing its molecular arrangement including a chlorophenyl group, linked aromatic rings, and ester functional groups.*
FDA Label Image

50 mg 90 Ct (Fenofibrate Tablets 54 mg And 160 mg 0115 2)

50 mg 90 Ct (Fenofibrate Tablets 54 mg And 160 mg 0115 2)
Label for Fenofibrate Tablets 54 mg by Amneal Pharmaceuticals LLC. The label states each tablet contains 54 mg fenofibrate and includes storage instructions (20° to 25°C), dosage caution, child-resistant container details, and a warning about the safety seal. The package contains 90 tablets. Barcodes and distributor address in Bridgewater, NJ, are also visible.*
FDA Label Image

1 (Fenofibrate Tablets 54 mg And 160 mg 0115 3)

1 (Fenofibrate Tablets 54 mg And 160 mg 0115 3)
Label for Fenofibrate Tablets 160 mg oral tablets by Amneal Pharmaceuticals. The label indicates 90 tablets per container, with storage instructions to keep between 20° to 25°C. It includes dosage instructions to see accompanying information, warnings about the safety seal, and container requirements. The label also shows a barcode and the NDC number 0115-5522-10.*

* 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.