Decitabine Injection, Powder, Lyophilized, For Solution
Product Images NDC 68083-528

3 FDA label images from Gland Pharma Limited · 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 68083-528). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Decitabine-spl-carton-label (Decitabine Spl Carton Label)

Decitabine-spl-carton-label (Decitabine Spl Carton Label)
Decitabine for Injection 50 mg per vial packaging label for lyophilized powder injection, intended for intravenous infusion only. Includes warnings about cytotoxicity, storage instructions to keep at 20°C to 25°C, and manufacturer information for Gland Pharma Limited, India. The label details reconstitution instructions and dosage information.*
FDA Label Image

Decitabine-spl-structure (Decitabine Spl Structure)

Decitabine-spl-structure (Decitabine Spl Structure)
Chemical structure of decitabine showing its molecular framework including a pyrimidine ring and a sugar moiety with labeled carbon positions.*
FDA Label Image

Decitabine-spl-vial-label (Decitabine Spl Vial Label)

Decitabine-spl-vial-label (Decitabine Spl Vial Label)
Label for Decitabine for Injection 50 mg per vial, a lyophilized powder for intravenous infusion. The single-dose sterile vial is a cytotoxic agent, manufactured by Gland Pharma Limited in India. Storage instructions are to keep at 20°C to 25°C, and it includes warnings about discarding unused portions. The label also shows the product NDC 68083-528-01 and space for lot and expiration details.*

* 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.