Structural Formula (Azathioprine Sodium For Injection Usp 1)
Azathioprine Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9566
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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 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.
Figure 1 (Azathioprine Sodium For Injection Usp 2)
Azathioprine Sodium is a prescription drug for intravenous use only. It is a sterile lyophilized material that comes in vials containing 100 mg azathioprine sodium, which is equivalent to azathioprine, with sodium hydroxide and hydrochloric acid to adjust pH if needed. The usual dosage should be read on the package insert. To prepare a solution, 10 mL Sterile Water for Injection is injected into the vial and swirled until a clear solution is obtained, and it should be used within 24 hours. It is important to protect it from light and store it in the carton at 20-25°C (68-77°F). The manufacturer is THYMOORGAN PHARMAZIE GmbH, Germany, and it is distributed by WEST-WARD in Eatontown, NJ 07724, USA.*
Vial Label For Azathioprine Sodium 100 mg (Azathioprine Sodium For Injection Usp 3)
This is a text that appears to contain product identification and tracking information. Specifically, it includes a T Lot identifier, an expiration date, and a code for a Global Trade Item Number (GTIN) as well as a serial number (SN). Without additional context, it is difficult to determine what the product is or what industry it may be associated with.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
