Lorazepam Tablet
Product Images NDC 63304-772

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lorazepam (NDC 63304-772). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries 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

1 (Spl Lorazepam Tablet Structure)

Chemical structure diagram of Lorazepam, a benzodiazepine active ingredient with chlorine-substituted aromatic rings and characteristic seven-membered diazepine ring with hydroxyl and ketone functional groups, illustrating its molecular framework.*

FDA Label Image

Label, 0.5 mg, 100 Tablets (Spl Lorazepam Tablet Label 0.5 mg)

Lorazepam Tablets, USP 0.5 mg oral tablets label by Sun Pharmaceutical Industries Inc. The label includes the dosage strength of 0.5 mg and states the package contains 90 tablets. It features the Rx only designation, a Schedule IV symbol, and instructs pharmacists to dispense with a medication guide. Manufacturer and distributor details for Ohm Laboratories Inc. and Sun Pharmaceutical Industries are also visible.*

FDA Label Image

Label, 1 mg, 100 Tablets (Spl Lorazepam Tablet Label 1mg)

Lorazepam Tablets USP 1 mg oral tablets label from Sun Pharmaceutical Industries Inc. The label includes dosage strength (1 mg), medication guide dispensing instructions, prescription-only status, and a package count of 90 tablets. Additional labeling includes storage instructions, manufacturer and distributor details, and barcodes. A designated 'Non Varnish Area' is marked on the right side of the label.*

FDA Label Image

Label, 2 mg, 100 Tablets (Spl Lorazepam Tablet Label 2 mg)

Lorazepam Tablets, USP 2 mg oral tablets label from Sun Pharmaceutical Industries Inc. The label indicates a package containing 90 tablets with an NDC of 63304-774-90. It includes dispensing instructions for pharmacists and storage guidelines, noting the product is Rx only.*

* 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.