Azathioprine Tablet
Product Images NDC 72789-129

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Azathioprine (NDC 72789-129). 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

72789129 Label (72789129)

The image shows the label for AZATHIOPRINE tablets, 50 mg strength, containing 30 tablets per bottle. The label includes warnings to keep the drug out of reach of children and dosage instructions in both English and Spanish. The product is manufactured by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK, with NDC 72789-129-30. Additional details include lot number J20A94 and expiration date 07/2022.*

FDA Label Image

1 (Azathioprine Tablets Usp 1)

Chemical structure diagram of azathioprine, showing its molecular framework including nitrogen, sulfur, and other atoms arranged in ring formations corresponding to the active ingredient azathioprine.*

* 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.