Lorazepam Tablet
Product Images NDC 71610-655

View Photos of 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 Lorazepam (NDC 71610-655). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Bottle Label 0.5 mg (71610 0654 10)

Bottle Label 0.5 mg (71610 0654 10)
Lorazepam USP 0.5 mg tablet label showing a bottle containing 10 tablets. The label includes the NDC number 71610-0654-10, storage instructions to keep at controlled room temperature, manufacturer listed as Aphena Pharma Solutions - Tennessee, LLC, and distributor as TEVA Czech Industries. Additional details include lot number, expiration date, and a warning that the product is RX only.*
FDA Label Image

Bottle Label 2 mg (71610 0655 30)

Bottle Label 2 mg (71610 0655 30)
Lorazepam USP 2 mg oral tablets label indicates a bottle containing 30 tablets. The label shows the NDC number 71610-0655-30, storage instructions to keep between 20-25 degrees Celsius, and cautions to keep the medicine out of the reach of children. It is labeled for prescription use only and manufactured by Aphena Pharma Solutions - Tennessee, LLC in Cookeville, TN.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

1 (Lorazepam Tablets A072926 A072927 A072928 1)

1 (Lorazepam Tablets A072926 A072927 A072928 1)
Chemical structure of lorazepam showing its molecular formula C15H10Cl2N2O2 and molecular weight 321.16. The structure includes two chlorine atoms, a benzodiazepine core, and other characteristic functional groups.*

* 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.