Ezetimibe Tablet
Product Images NDC 33342-373

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ezetimibe (NDC 33342-373). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods 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

225 (Ezetimibe 30s)

Ezetimibe Tablets USP 10 mg oral tablets packaging label by Macleods Pharmaceuticals Limited. The label indicates each uncoated tablet contains 10 mg Ezetimibe, with usual dosage of one tablet daily. It is a 30-tablet package, manufactured in Baddi, Himachal Pradesh, India, and distributed by Macleods Pharma USA, Inc.*

FDA Label Image

000 (Ezetimibe 500s)

Ezetimibe 10 mg tablets packaging label by Macleods Pharmaceuticals Limited shows a bottle label for oral tablets containing 10 mg of Ezetimibe. The label indicates 500 tablets in bulk packaging, storage instructions, dosage directions, and manufacturer details for Macleods Pharma USA, Inc.*

FDA Label Image

110 (Ezetimibe 90s)

Label for Ezetimibe 10 mg oral tablets, containing 90 tablets per package. The label displays Macleods Pharmaceuticals Limited as the manufacturer. It includes storage instructions, dosage information, and barcodes on a white background with black and green text.*

FDA Label Image

Ezetimibe-structure.jpg (Ezetimibe Structure)

Chemical structure of Ezetimibe, showing its molecular framework including a fluorophenyl group, a hydroxyl group, and a beta-lactam ring with sulfur and nitrogen atoms.*

* 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.