Ezetimibe Tablet
Product Images NDC 10135-787

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ezetimibe (NDC 10135-787). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex 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

Structural Formula (Image 01)

Chemical structure of the active ingredient Ezetimibe showing its molecular arrangement including aromatic rings, fluorine atoms, hydroxyl groups, and a beta-lactam ring system.*

FDA Label Image

1 (Label 1)

Label for Ezetimibe 10 mg tablets by Marlex Pharmaceuticals, Inc. The label indicates oral administration with 30 tablets per bottle. The label includes dosage information, storage instructions, and a barcode. The product is marked as prescription only.*

FDA Label Image

2 (Label 2)

Ezetimibe Tablets USP 10 mg oral tablets packaging label. The label shows Marlex Pharmaceuticals, Inc. as the manufacturer and distributor, with a 90-tablet count. It includes dosage information, storage instructions, a barcode, and a note indicating prescription use only.*

FDA Label Image

3 (Label 3)

Label for Ezetimibe Tablets USP 10 mg by Marlex Pharmaceuticals, Inc. The label states the product contains 500 tablets for oral use, prescription only. Storage instructions specify 25°C (77°F) with permitted excursions to 15-30°C (59-86°F), and protection from moisture. The label includes a barcode and manufacturing details.*

* 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.