Azacitidine Injection, Powder, Lyophilized, For Solution
Product Images NDC 60505-6271

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Azacitidine (NDC 60505-6271). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp, 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

Carton (Carton)

Azacitidine for Injection 100 mg per vial in lyophilized powder form for solution, labeled for subcutaneous and intravenous use. The single-dose vial package includes warnings for cytotoxic agents and storage instructions. Manufactured by Jiangsu Hansoh Pharmaceutical Group Co., Ltd. and distributed by Apotex Corp, Weston Florida, USA. The label notes dilution required and single-dose vial use only.*

FDA Label Image

Figure 1 (Figure 1)

A Kaplan-Meier survival curve showing proportion surviving over time in months from randomization comparing two groups labeled AZA and CCR. The graph includes hazard ratio, confidence interval, p-value, and number at risk for each group over time.*

FDA Label Image

Structure (Structure)

Chemical structure of azacitidine showing the molecular arrangement of its atoms including nitrogen, oxygen, and hydroxyl groups in the ring and attached side chains.*

FDA Label Image

Flat Label (Flat Label)

Label of Azacitidine for Injection, 100 mg per vial, for subcutaneous and intravenous use only. It is a lyophilized powder requiring dilution, indicated as a single-dose vial. The label includes warnings for cytotoxicity, manufacturer Jiangsu Hansoh Pharmaceutical Group Co., and distributor Apotex Corp.*

* 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.