Fenofibrate Tablet
Product Images NDC 82619-102

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 82619-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Creekwood Pharmaceuticals 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

Image Description (Fenofibrate Tablets Usp 120mg)

Image Description (Fenofibrate Tablets Usp 120mg)
Label for Fenofibrate Tablets USP 120 mg, a prescription oral tablet from Creekwood Pharmaceuticals LLC. The label states a package count of 90 tablets, dosage details, storage instructions, and manufacturer information (V-Ensure Pharma Technologies Pvt. Ltd., India). It includes standard warnings such as keeping out of reach of children and using a child-resistant container.*
FDA Label Image

Image Description (Fenofibrate Tablets Usp 40mg)

Image Description (Fenofibrate Tablets Usp 40mg)
Label for Fenofibrate Tablets USP 40 mg, oral tablets, containing 90 tablets per bottle. The label includes dosage instructions, storage conditions (20° to 25°C), and warnings to keep out of reach of children. Manufactured by V-Ensure Pharma Technologies Pvt. Ltd. and distributed by Creekwood Pharmaceuticals LLC.*
FDA Label Image

Structure (E1f9aae1 Cd76 4449 A092 0202d95fced1 01)

Structure (E1f9aae1 Cd76 4449 A092 0202d95fced1 01)
Chemical structure of fenofibrate, the active ingredient in FENOFIBRATE tablets. The diagram shows the molecular arrangement including chlorine and ester functional groups characteristic of fenofibrate.*

* 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.