Alprazolam Tablet
Product Images NDC 72789-313

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alprazolam (NDC 72789-313). 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

1 (Image 1)

Alprazolam 0.5 mg oral tablets in a white blister card with a yellow and white cardboard sleeve. The sleeve and blister card are labeled with the product name Alprazolam, strength 0.5 mg, tablet dosage form, and include markings from PD-Rx Pharmaceuticals, Inc. The package contains 1 tablet. The label displays the National Drug Code 72789-313.*

FDA Label Image

1 (Image 5)

Chemical structure of alprazolam showing its triazolobenzodiazepine core with a chlorine-substituted benzene ring, a methyl group, and additional nitrogen atoms in the fused ring system.*

FDA Label Image

1 (Image 6)

Alprazolam 0.5 mg oral tablets in a white plastic bottle with a white child-resistant cap. The label displays the product name Alprazolam, strength 0.5 mg, quantity 100 tablets, and is labeled by PD-Rx Pharmaceuticals, Inc.*

FDA Label Image

72789313 Label (72789313)

Label for Alprazolam USP 0.5 mg oral tablets, containing 90 tablets per bottle. The label includes the NDC 72789-313-90 and is labeled by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. It features dosage strength, quantity, lot number C23C28, and expiration date 06/2025. The label includes warnings and usage instructions in both English and Spanish.*

* 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.