Alprazolam Tablet
Product Images NDC 72789-328

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alprazolam (NDC 72789-328). 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

72789328 Label (72789328)

Label for Alprazolam USP 1 mg oral tablets, packaged as 30 tablets per bottle. The label includes directions for dosage and storage, warnings to keep out of reach of children, and a notice about avoiding alcohol. The product is manufactured or labeled by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK, with NDC 72789-328-30. Additional details include lot number F23B96 and expiration date 07/2025.*

FDA Label Image

1 (Image 1)

Alprazolam 1 mg oral tablet blister pack from PD-Rx Pharmaceuticals, Inc. The silver foil pack shows the product name and dosage strength repeated across each tablet cavity. No further text or branding is visible on the blister itself.*

FDA Label Image

1 (Image 5)

Chemical structure diagram of Alprazolam, the active ingredient in the drug product. The structure depicts a triazolobenzodiazepine core with a chlorine-substituted benzene and other characteristic rings consistent with Alprazolam.*

FDA Label Image

1 (Image 6)

Alprazolam 1 mg oral tablets packaged in a white and blue blister card by PD-Rx Pharmaceuticals, Inc. Each blister card contains 50 tablets arranged in 5 rows of 10 tablets each. The label includes the product name Alprazolam and the dosage strength 1 mg, along with identification codes and manufacturing details.*

* 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.