Fenofibrate Tablet, Film Coated
Product Images NDC 46708-554

View Photos of 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 46708-554). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals 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

90 Tablets (Fenofibrate 160mg)

90 Tablets (Fenofibrate 160mg)
This is a description of Fenofibrate Tablet, which contains 160 mg of fenofibrate in each film-coated tablet. The standard dosage is mentioned in the package insert for complete prescribing details. It is suggested that the tablet should be stored at the temperature range between 20° to 25°C and should be protected from moisture. The drug is produced by Alembic Pharmaceuticals Limited (Formulation Division), in Gujarat, India. Each bottle comes with 90 tablets, and it can be prescribed by a physician only. It is essential to keep these drugs out of the reach of children. The text also mentions the manufacturing license number and NDC code for the drug.*
FDA Label Image

90 Tablets (Fenofibrate 54mg)

90 Tablets (Fenofibrate 54mg)
This is a description of a medication called Fenofibrate. Each tablet is coated with 54mg of Fenofibrate, USP. The package insert should be referred to for dosage information, and the medication should be stored within specific temperature conditions and protected from moisture. Fenofibrate Tablets, USP are manufactured by Alembic Pharmaceuticals Limited, and come in a bottle with 90 tablets. The medication should be dispensed in a tight, light-resistant container as defined in the USP with a child-resistant closure as required. Lastly, it has a Manufacturing License Number of G1959 and an NDC number of 46708-554-90.*
FDA Label Image

Structure (Fenofibrate Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.