Azacitidine Injection, Powder, Lyophilized, For Solution
Product Images NDC 16714-927

View Photos of 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 Azacitidine (NDC 16714-927). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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)

Carton (Carton)
Azacitidine is a medication for injection indicated for subcutaneous and intravenous use. The medication is found in a sterile single-dose vial containing 100mg/vial of azacitidine and mannitol. Azacitidine should be diluted before use and the dosage should be determined according to the prescribing information. The unused portion should be discarded and kept out of reach of children. The medication should be stored within the range of 20°C to 25°C (68°F to 77°F).*
FDA Label Image

Vial (Vial)

Vial (Vial)
This is a description of a single-dose vial of Azacitidine for Injection. It comes in a 100mg/vial strength and must be diluted. The vial contains azacitidine 100mg and mannitol 100mg. The usual dosage is advised to be determined from the prescribing information for dosing and administration. It's meant for subcutaneous and intravenous use only, and unused portions should be discarded. The vial must be stored between 20°C to 25°C (68°F to 77°F). The manufacturing company is Northstar Rx LLC in Memphis, TN, and it was made by Dr. Reddy's Laboratories Limited in Visakhapatnam, India.*
FDA Label Image

Graph (Graph)

Graph (Graph)
This is a statistical analysis of a medical study with two groups of patients treated with different therapies. The Log-Rank test yielded a p-value of 0.0001, indicating a significant difference in survival between the two groups. The Hazard Ratio (HR) for the treatment being evaluated is 0.58 with a 95% confidence interval of 0.43 to 0.77. The number of deaths in each group is provided (82 in the Aza group and 113 in the CCR group), and a survival curve is presented graphically, showing the proportion of patients surviving over time for each group. The X-axis represents time in months, and the Y-axis represents the proportion of patients. The number of patients "at risk" at each time point is also provided for each group.*
FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.