Decitabine Injection, Powder, Lyophilized, For Solution
Product Images NDC 75834-190

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Decitabine (NDC 75834-190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nivagen Pharmaceuticals, 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.

FDA Label Image

Carton (Decitabine For Injection 50mg Vial Cartonc2c 50)

Packaging label for DECITABINE 50 mg per vial injection, a lyophilized powder for intravenous infusion. The label states it is a single dose vial for intravenous use only, manufactured by Nivagen Pharmaceuticals, Inc. The label includes warnings about cytotoxicity, reconstitution instructions, storage conditions, and a barcode with NDC 75834-190-01. The product is made in Argentina.*

FDA Label Image

Vial (Decitabine For Injection 50mg Vial Labelc2c 75)

Label for DECITABINE for Injection 50 mg per vial, a lyophilized powder for intravenous infusion. The label includes usage warnings such as 'Cytotoxic Agent' and 'Single Dose Vial.' It lists the NDC number 75834-190-01 and the labeler, Nivagen Pharmaceuticals, Inc. Additional storage and preparation instructions are present, along with a barcode and a note indicating space for validation without tamper-evident features.*

FDA Label Image

Structure (Decitabine Structure)

Chemical structure diagram of decitabine showing the arrangement of atoms including nitrogen, oxygen, hydrogen, and carbon in the molecule. The structure highlights the sugar moiety linked to a heterocyclic ring with labeled atomic positions.*

* 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.