Ezetimibe Tablet
Product Images NDC 51660-200

4 FDA label images from Ohm Laboratories Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ezetimibe (NDC 51660-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ohm Laboratories 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

Structure (Ezetimibe 1)

Structure (Ezetimibe 1)
Chemical structure of the active ingredient Ezetimibe, showing its molecular configuration with functional groups and aromatic rings.*
FDA Label Image

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Label for Ezetimibe Tablets USP 10 mg by Ohm Laboratories Inc. The label indicates the product is a prescription oral tablet, with 30 tablets per container. It includes dosage instructions, storage information, and manufacturer details, along with barcode and NDC 51660-200-30.*
FDA Label Image

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The label for Ezetimibe Tablets USP 10 mg oral tablets by Ohm Laboratories Inc. It indicates the product is prescription only and contains 90 tablets per container. The label includes storage instructions, manufacturer and distributor information, NDC 51660-200-90, and barcode graphics. The label also notes a non-varnish area on one end.*
FDA Label Image

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Label for Ezetimibe Tablets USP 10 mg oral tablets by Ohm Laboratories Inc. The label specifies 500 tablets per container and includes usage, storage, and handling instructions along with manufacturer and distributor information. The label also features multiple barcodes and a note for non-varnish area.*

* 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.