Decitabine Injection, Powder, Lyophilized, For Solution
Product Images NDC 70121-1644

3 FDA label images from Amneal Pharmaceuticals 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 70121-1644). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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.

FDA Label Image

Structure (Decitabine Amneal 01)

Structure (Decitabine Amneal 01)
Chemical structure diagram of decitabine, showing its molecular arrangement including labeled positions on the nitrogenous base and the sugar moiety typical of nucleoside analogs.*
FDA Label Image

Vial Label (Decitabine Amneal 02)

Vial Label (Decitabine Amneal 02)
Decitabine for Injection 50 mg per vial packaging label by Amneal Pharmaceuticals LLC. The label displays that the vial contains 50 mg decitabine as lyophilized powder for intravenous infusion, along with ingredients and storage instructions. It is a single-dose, sterile vial labeled for prescription use only, with barcode and lot/expiration fields included.*
FDA Label Image

Carton Label (Decitabine Amneal 03)

Carton Label (Decitabine Amneal 03)
Label for Decitabine for Injection 50 mg per vial by Amneal Pharmaceuticals LLC. The label includes dosing instructions for reconstitution and warnings about the product being a cytotoxic agent intended for intravenous infusion only. Storage and stability information are also noted, along with barcodes and lot identification areas. The design uses black text with magenta highlight boxes and features the Amneal logo at the bottom.*

* 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.