Fenofibrate Tablet, Film Coated
Product Images NDC 62332-350

3 FDA label images from Alembic Pharmaceuticals 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 62332-350). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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

Fenofibrate-160mg.jpg (Fenofibrate 160mg)

Fenofibrate-160mg.jpg (Fenofibrate 160mg)
Fenofibrate Tablets, USP 160 mg film-coated tablets label from Alembic Pharmaceuticals Inc. The label indicates prescription use, packaging of 30 tablets, storage instructions, manufacturer details, and includes a barcode and NDC 62332-351-30.*
FDA Label Image

Fenofibrate-54mg.jpg (Fenofibrate 54mg)

Fenofibrate-54mg.jpg (Fenofibrate 54mg)
The packaging label for Fenofibrate Tablets, USP 54 mg by Alembic Pharmaceuticals Inc. shows a film-coated tablet count of 30. It includes storage instructions, dosage advisories, manufacturing information for Alembic Pharmaceuticals Limited (India) and Alembic Pharmaceuticals, Inc. (USA), a barcode, and regulatory details such as Rx only and various codes for labeling and identification.*
FDA Label Image

Fenofibrate Structure.jpg (Fenofibrate Structure)

Fenofibrate Structure.jpg (Fenofibrate Structure)
Chemical structure of Fenofibrate showing its molecular composition and arrangement, including a chlorophenyl group, ketone, and ester 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.