Fenofibrate Tablet, Film Coated
Product Images NDC 59651-576

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 59651-576). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Figure 1 (Fenofibrate Fig 1)

Fenofibrate Tablets USP 54 mg film-coated oral tablets label from Aurobindo Pharma Limited. The label specifies 90 tablets per container, with storage instructions and safety warnings. It includes the NDC 59651-575-90 and distributor information for Aurobindo Pharma USA, Inc.*

FDA Label Image

Figure 2 (Fenofibrate Fig 2)

Label for Fenofibrate Tablets, USP 160 mg oral film-coated tablets by Aurobindo Pharma Limited. The label indicates a package size of 90 tablets with dosage strength of 160 mg. The label includes storage instructions, distributor information for Aurobindo Pharma USA Inc., and regulatory disclaimers. A single tablet image embossed with '160' is shown.*

FDA Label Image

Chemical Structure (Fenofibrate Str)

Chemical structure diagram of Fenofibrate, showing its molecular composition with chlorine, benzene rings, and ester groups as part of its chemical formula.*

* 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.