Fenofibrate Capsule
Product Images NDC 62135-893

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 62135-893). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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 Caps 134mg Bottel Label)

Fenofibrate Capsules, USP 134 mg oral capsules in a package containing 90 capsules. The label indicates Rx Only and is manufactured by Chartwell Rx, LLC. The label includes usage and storage instructions and a barcode with the NDC 62135-894-90.*

FDA Label Image

Image Description (Fenofibrate Caps 200mg Bottel Label)

Label for Fenofibrate Capsules, USP, 200 mg strength, oral capsules manufactured by Chartwell RX, LLC. The label indicates a package count of 90 capsules and specifies storage and usage instructions along with the National Drug Code (NDC) 62135-899. The label includes a barcode and safety warnings to keep medication out of reach of children.*

FDA Label Image

Image Description (Fenofibrate Caps 67mg Bottel Label)

Fenofibrate 67 mg Capsules, USP label from Chartwell RX, LLC. The packaging indicates 90 capsules per bottle, Rx only, with storage instructions between 20°C to 25°C. It includes a barcode and a warning to keep all medications out of reach of children. The label mentions the capsules are in child-resistant containers and to not accept if the seal is broken or missing.*

FDA Label Image

Image Description (Fenofibrate Caps Structure)

Chemical structure of fenofibrate depicting the molecular arrangement including chlorine-substituted benzene ring, ester linkages, and multiple methyl 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.