Azathioprine
Product Images NDC 54868-5310

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Azathioprine (NDC 54868-5310). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Structured Formula For Azathioprine Tablets (5310)

Structured Formula For Azathioprine Tablets (5310)
Label for Azathioprine 50 mg tablets from Physicians Total Care, Inc. The package contains 60 tablets. The label includes dosage information, caution about prescription dispensing, storage instructions to keep at controlled room temperature, and a lot number and expiration date. A barcode and NDC 54868-5310-3 are also visible.*
FDA Label Image

Structure Formula For Azathioprine (Azathioprine Tablets Figure 01)

Structure Formula For Azathioprine (Azathioprine Tablets Figure 01)
Chemical structure diagram of Azathioprine, showing its molecular framework with nitrogen, sulfur, carbon, and oxygen atoms configured in a purine derivative structure.*
FDA Label Image

Structure Formula For Azathioprine02 (Azathioprine Tablets Figure 02)

Structure Formula For Azathioprine02 (Azathioprine Tablets Figure 02)
A biochemical pathway diagram illustrating the metabolism of Azathioprine. The diagram shows Azathioprine converting to 6-MP, which then follows different enzymatic routes and metabolites including 6-MeMP, 6-TU, TIMP, and 6-TGN, with key enzymes such as TPMT, XO, and HGPRT involved. The pathway also notes processes like inhibition of purine synthesis and incorporation into DNA.*

* 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.