Fenofibrate Tablet, Film Coated
Product Images NDC 69315-289

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 69315-289). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leading Pharma, 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

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Chemical structure of fenofibrate showing its molecular composition and arrangement of atoms, including chlorine, carbon, oxygen, and hydrogen atoms represented by standard chemical notation.*
FDA Label Image

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Label for Fenofibrate Tablets, USP 54 mg film-coated oral tablets by Leading Pharma, LLC. The bottle contains 90 tablets and is Rx only. Label includes storage instructions at 20° to 25°C, manufacturing details by Graviti Pharmaceuticals Pvt. Ltd., India, and barcode on the right.*
FDA Label Image

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Label for Fenofibrate Tablets USP 160 mg, film-coated oral tablets. The package contains 90 tablets and is manufactured for Leading Pharma, LLC. The label includes storage instructions, dosage information, and manufacturing details for Graviti Pharmaceuticals Pvt. Ltd., India, along with the NDC number 69315-290-09.*
FDA Label Image

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Label for Fenofibrate Tablets, USP 160 mg film-coated tablets, oral dosage form, with a total of 500 tablets. Manufactured for Leading Pharma, LLC, Fairfield, NJ, and by Graviti Pharmaceuticals Pvt. Ltd., India. The label includes storage instructions, dosage guidance referencing package insert, and a 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.