Alprazolam Tablet
Product Images NDC 72789-313

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 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

72789313 Label (72789313)

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.*
FDA Label Image

Image (Alprazolam Tabs Usp Goa Sunrise A074342 1)

Image (Alprazolam Tabs Usp Goa Sunrise A074342 1)
Alprazolam 0.5 mg oral tablets packaging label from PD-Rx Pharmaceuticals, Inc. The image shows a bottle with a red cap and a white label displaying the product name Alprazolam, strength of 0.5 mg, and the dosage form as tablets. The label also includes the barcode and the labeler name, PD-Rx Pharmaceuticals, Inc.*
FDA Label Image

1 (Alprazolam Tabs Usp Goa Sunrise A074342 5)

1 (Alprazolam Tabs Usp Goa Sunrise A074342 5)
Chemical structure of Alprazolam, showing its fused ring system including a benzodiazepine core with chlorine and methyl substituents.*

* 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.