Fenofibrate Tablet
Product Images NDC 69238-1260

3 FDA label images from Amneal Pharmaceuticals Ny 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 69238-1260). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

Formula (Fenofibrate Tablets Usp 48mg And 145mg 1)

Formula (Fenofibrate Tablets Usp 48mg And 145mg 1)
Chemical structure diagram of fenofibrate, showing its molecular composition with chloro-substituted phenyl rings and ester functional groups.*
FDA Label Image

48 mg (Fenofibrate Tablets Usp 48mg And 145mg 2)

48 mg (Fenofibrate Tablets Usp 48mg And 145mg 2)
Fenofibrate Tablets USP 48 mg oral tablets packaging label shows 90 tablets per bottle. Label includes NDC 69238-1260-9 and specifies each film-coated tablet contains 48 mg of fenofibrate. The labeler is Amneal Pharmaceuticals LLC, Bridgewater, NJ. Storage instructions and dispensing warnings are also visible.*
FDA Label Image

145 mg (Fenofibrate Tablets Usp 48mg And 145mg 3)

145 mg (Fenofibrate Tablets Usp 48mg And 145mg 3)
Fenofibrate Tablets, USP 145 mg film-coated oral tablets label from Amneal Pharmaceuticals NY LLC. The label includes dosage strength, storage instructions, usage warnings, quantity of 90 tablets, and distributor information with barcode and packaging details.*

* 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.