Fenofibrate Tablet, Film Coated
Product Images NDC 42385-935

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 42385-935). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laurus Labs Limited, 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

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Chemical structure of fenofibrate, showing its atomic arrangement including chlorine, carbon, oxygen, and hydrogen atoms connected by single and double bonds.*

FDA Label Image

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Label for Fenofibrate Tablets, USP 54 mg, film-coated oral tablets. The package contains 90 tablets and is labeled Rx only. Manufactured for Laurus Generics Inc. and by Graviti Pharmaceuticals Pvt. Ltd. The label includes storage instructions and a barcode.*

FDA Label Image

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Label for Fenofibrate Tablets USP 160 mg film-coated tablets by Laurus Labs Limited. The container holds 90 tablets. The label includes storage instructions at 20° to 25°C, dispensing instructions with child-resistant closure, and manufacturing details for Laurus Generics Inc. and Graviti Pharmaceuticals Pvt. Ltd. The label also features the Laurus Labs logo and an NDC barcode.*

* 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.