Ezetimibe Tablet
Product Images NDC 48433-161

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 Ezetimibe (NDC 48433-161). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safecor Health, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Ezetimibe Tablets, 10 mg (56f76598 4f3b 4d27 Bca3 057a6d287bb3 01)

Ezetimibe Tablets, 10 mg (56f76598 4f3b 4d27 Bca3 057a6d287bb3 01)
Chemical structure diagram of ezetimibe, showing its molecular configuration and atoms arrangement as part of the FDA labeling information.*
FDA Label Image

Ezetimibe Tablets, Usp 10 mg Unit Carton Label (Image 01)

Ezetimibe Tablets, Usp 10 mg Unit Carton Label (Image 01)
The label is for Ezetimibe tablets, USP, with a strength of 10 mg. It is an oral human prescription drug produced by Safecor Health, LLC. The label includes the NDC number 48433-161-03 and specifies the package contains 30 tablets (3 x 10). It also provides storage instructions and cautions for use, as well as manufacturer information including Zydus Lifesciences Ltd. and Zydus Pharmaceuticals (USA) Inc.*
FDA Label Image

Unit Carton (Image 02)

Unit Carton (Image 02)
Label panel for ezetimibe 10 mg oral tablet by Safecor Health, LLC. The blue label features the UDL logo with the tagline 'A Safecor Health Company.' Warnings note that the unit dose package is not child resistant, is for institutional use only, and provides light resistance. The label includes Safecor Health contact information and advises users to see the window for lot number and expiration date.*

* 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.