Fenofibrate
Product Images NDC 54868-5660

3 FDA label images from Physicians Total Care, Inc. · 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 54868-5660). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, Inc., 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

Principal Display Panel (160 mg Tablet Bottle Label)

Principal Display Panel (160 mg Tablet Bottle Label)
Fenofibrate 160 mg tablets packaging label from Physicians Total Care, Inc. The label indicates a quantity of 30 tablets and includes caution about federal law prohibiting dispensing without prescription. Additional regulatory and storage information, including lot number, expiration date, and manufacturer details, is visible on the label.*
FDA Label Image

Principal Display Panel (54 mg Tablet Bottle Label)

Principal Display Panel (54 mg Tablet Bottle Label)
Label for Fenofibrate 54 mg tablet distributed by Physicians Total Care, Inc., Tulsa, OK. The label includes the National Drug Code (NDC) 54868-5697-0, batch number LOT #0000, and expiration date 01/60. Manufactured by Ippon Laboratories, Inc. in Maynard, CA.*
FDA Label Image

Chemical Structure (Fenofibrate 01)

Chemical Structure (Fenofibrate 01)
Chemical structure of the active ingredient Fenofibrate, showing its molecular arrangement with a chlorophenyl group, ester, and ketone functional groups.*

* 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.