Lorazepam Tablet
Product Images NDC 72789-357

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lorazepam (NDC 72789-357). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

Image (72789355)

Lorazepam Tablets USP 0.5 mg oral tablets packaging label by PD-Rx Pharmaceuticals, Inc. The label indicates each scored tablet contains 0.5 mg of lorazepam. It includes storage instructions to keep at 20-25°C and to dispense in a child-resistant container. The package contains 1000 tablets, marked for Rx only, with manufacturer OHM Laboratories Inc. The label displays the NDC 72789-355-95 and includes barcode and lot/expiration details.*

FDA Label Image

Image (72789356)

Lorazepam Tablets USP 1 mg oral tablets, marketed and packaged by PD-Rx Pharmaceuticals, Inc., with a package containing 1000 tablets. The label shows the NDC code 72789-356-95, an indication of the dosage strength (1 mg), and the drug classification (Schedule IV). It includes storage instructions and manufacturer information from OHM Laboratories Inc.*

FDA Label Image

Image (72789357)

Lorazepam Tablets USP 2 mg oral tablets packaging label from PD-Rx Pharmaceuticals, Inc. This container holds 90 scored tablets. The label includes storage instructions, dispensing guidance, NDC 72789-357-90, and manufacturer information for OHM Laboratories Inc. in New Brunswick, NJ.*

FDA Label Image

1 (Spl Lorazepam Tablet Structure)

Chemical structure diagram of lorazepam, showing its molecular framework including chlorinated aromatic rings and functional groups characteristic of the compound.*

* 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.