Azathioprine
Product Images NDC 71610-306

4 FDA label images from Aphena Pharma Solutions - Tennessee, Llc · 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 Azathioprine (NDC 71610-306). 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 50 mg (71610 0306 60)

Bottle Label 50 mg (71610 0306 60)
Azathioprine 50 mg tablets label by Aphena Pharma Solutions - Tennessee, LLC. The label shows the drug name, strength, NDC 71610-0306-60, quantity of 90 tablets, storage instructions to keep between 20-25°C and to store in the original container, and manufacturer information including Aphena Pharma Services Corp. located in Wilmington, NC, and packaging by Aphena Pharma in Cookeville, TN. The label also includes lot number, expiration date, and barcodes.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Aza01-0000-01.jpg (Aza01 0000 01)

Aza01-0000-01.jpg (Aza01 0000 01)
Chemical structure of Azathioprine illustrating its molecular arrangement with labeled atoms and bonds.*
FDA Label Image

Aza01-0000-02.jpg (Aza01 0000 02)

Aza01-0000-02.jpg (Aza01 0000 02)
A biochemical pathway diagram illustrating the metabolism of Azathioprine. It shows Azathioprine converting through several intermediates, including 6-MP, TIMP, and other metabolites involved in DNA synthesis inhibition and incorporation into DNA. Enzymes like TPMT, HPRT, and XO are identified at various steps in the pathway.*

* 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.