Decitabine Injection, Powder, Lyophilized, For Solution
Product Images NDC 55150-376

3 FDA label images from Eugia Us Llc · 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 Decitabine (NDC 55150-376). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, 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

Package Label-principal Display Panel-50 mg Per Vial (Container Label)

Package Label-principal Display Panel-50 mg Per Vial (Container Label)
Label for Decitabine for Injection 50 mg per vial, a lyophilized powder for intravenous infusion. The label includes dosage and storage information, a warning that it is a cytotoxic agent, and manufacturer details for AuroMedics Pharma LLC. The vial is single-dose and sterile, with a note to discard any unused portion.*
FDA Label Image

Package Label-principal Display Panel-50 mg Per Vial (Container-Carton (1 Vial))

Package Label-principal Display Panel-50 mg Per Vial (Container-Carton (1 Vial))
Packaging label for Decitabine Injection 50 mg per vial, a lyophilized powder for intravenous infusion. The label includes usage and storage instructions, a cytotoxic agent warning, and states it is a single-dose sterile vial. The labeler is Auromedics Pharma LLC, with distribution address in New Jersey. The NDC is 55150-376-01.*
FDA Label Image

Chemical Structure (Decitabine Str)

Chemical Structure (Decitabine Str)
Chemical structure diagram of Decitabine showing its molecular framework with labeled nitrogen, oxygen, and hydrogen atoms, including the sugar ring and base components.*

* 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.