Lorazepam Tablet
Product Images NDC 62135-862

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lorazepam (NDC 62135-862). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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.

FDA Label Image

Image Description (Lorazepam Tabs Usp 0pt5mg Bottle Label)

Packaging label for Lorazepam Tablets USP 0.5 mg oral tablets, supplied in a package of 100 tablets. The label includes dosing information, storage instructions, and the manufacturer Chartwell Rx. It also features the controlled substance schedule IV symbol and barcode.*

FDA Label Image

Image Description (Lorazepam Tabs Usp 1mg Bottle Label)

Lorazepam 1 mg Tablets USP packaging label for oral administration by Chartwell RX, LLC. The label shows a carton containing 100 tablets with a Schedule IV designation, the NDC 62135-862-01, and instructions for storage between 20°C to 25°C. It includes dispensing guidance and a barcode.*

FDA Label Image

Image Description (Lorazepam Tabs Usp 2mg Bottle Label)

Lorazepam 2 mg tablets packaging label. The label shows the product name Lorazepam Tablets, USP, strength 2 mg, and quantity of 100 tablets. It includes dispensing instructions, manufacturer Chartwell Rx, and a barcode. Features a green and blue color scheme with a note about a Medication Guide for the patient.*

FDA Label Image

Image Description (Lorazepam Tabs Usp Structure)

Chemical structure of lorazepam, a benzodiazepine derivative with chlorine substituents and hydroxyl group, shown as a molecular diagram with labeled atoms and bonds.*

* 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.