Fenofibrate Tablet, Film Coated
Product Images NDC 62332-361

2 FDA label images from Alembic Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 62332-361). 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 145 mg

Fenofibrate 145 mg
The packaging label for Fenofibrate Tablets, USP 145 mg, film-coated oral tablets by Alembic Pharmaceuticals Inc. The label states 30 tablets per bottle, prescription use only. It includes storage instructions, manufacturer details from Alembic Pharmaceuticals Limited in India and Alembic Pharmaceuticals, Inc. USA, the NDC 62332-361-30, and barcodes.*
FDA Label Image

Fenofibrate 48 mg

Fenofibrate 48 mg
Label for Fenofibrate Tablets, USP 48 mg by Alembic Pharmaceuticals Inc. The film-coated oral tablets come in a container of 30 tablets. The label includes storage instructions at 25°C with allowed excursions, a barcode, and manufacturer information for Alembic Pharmaceuticals Limited, Gujarat, India, and Alembic Pharmaceuticals Inc., Bedminster, NJ, USA.*

* 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.