Decitabine Injection, Powder, Lyophilized, For Solution
Product Images NDC 31722-304

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 Decitabine (NDC 31722-304). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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
FDA Label Image

Decitabineforinjcartonlabel (Decitabineforinjcartonlabel)

Decitabineforinjcartonlabel (Decitabineforinjcartonlabel)
Packaging label for Decitabine for Injection 50 mg per vial by Camber Pharmaceuticals, Inc. The label indicates intravenous infusion use and warns that it is a cytotoxic agent. Storage instructions specify temperatures between 20°C to 25°C with permitted excursions. Manufacturer details include HETERO Labs Limited, India. The label includes batch coding and barcode information.*
FDA Label Image

Decitabineforinjstructure (Decitabineforinjstructure)

Decitabineforinjstructure (Decitabineforinjstructure)
Chemical structure diagram of Decitabine, showing the molecular arrangement of the active ingredient Decitabine.*
FDA Label Image

Decitabineforinjviallabel (Decitabineforinjviallabel)

Decitabineforinjviallabel (Decitabineforinjviallabel)
Decitabine for Injection 50 mg per vial label from Camber Pharmaceuticals, Inc. The label indicates it is a single-dose sterile vial for intravenous infusion only. It includes dosage strength, storage instructions, and a cytotoxic agent warning. The label also provides manufacturer and contact details, with a barcode on the right side.*

* 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.