Azathioprine Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9566

3 FDA label images from Hikma Pharmaceuticals Usa Inc. · 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 Azathioprine Sodium (NDC 0143-9566). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Azathioprine Sodium For Injection Usp 1)

Structural Formula (Azathioprine Sodium For Injection Usp 1)
Chemical structure of Azathioprine Sodium, showing the molecular arrangement including a purine base, a nitroimidazole group, and the sodium ion.*
FDA Label Image

Figure 1 (Azathioprine Sodium For Injection Usp 2)

Figure 1 (Azathioprine Sodium For Injection Usp 2)
Azathioprine Sodium for Injection, USP 100 mg/vial, sterile lyophilized powder for intravenous use. The label includes dosage preparation instructions, storage conditions (20 to 25°C), and manufacturer info: THYMOORGAN PHARMAZIE GmbH, Germany, and distributor WEST-WARD, Eatontown, NJ USA. NDC 0143-9566-01. The label also emphasizes use under prescription and protecting from light.*
FDA Label Image

Vial Label For Azathioprine Sodium 100 mg (Azathioprine Sodium For Injection Usp 3)

Vial Label For Azathioprine Sodium 100 mg (Azathioprine Sodium For Injection Usp 3)
Label showing barcode and identifying information including lot number, expiration date, GTIN, and serial number for Azathioprine Sodium injection, powder, lyophilized, for solution, 100 mg/10 mL by Hikma Pharmaceuticals USA Inc.*

* 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.