Nelarabine Injection
Product Images NDC 39822-0650

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 Nelarabine (NDC 39822-0650). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xgen Pharmaceuticals Djb, 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

Nelarabine-label (Label)

Nelarabine-label (Label)
Nelarabine Injection 250 mg/50 mL (5 mg/mL) in a single-dose vial for intravenous infusion. The label states it is for infusion only and to discard any unused portion. It is manufactured by XGen Pharmaceuticals DJB, Inc., Big Flats, NY. The label includes storage instructions, formulation details, and a barcode.*
FDA Label Image

Nelarabine-multi-carton (Multi Carton)

Nelarabine-multi-carton (Multi Carton)
Nelarabine Injection 250 mg/50 mL (5 mg/mL) intravenous infusion packaging label from XGen Pharmaceuticals DJB, Inc. The label indicates 6 single-dose vials of 50 mL each. The box includes dosing strength, usage instructions to discard unused portion, storage conditions, and manufacturing details.*
FDA Label Image

Image Description (Nelarabine Figure 01)

Image Description (Nelarabine Figure 01)
Chemical structure of Nelarabine showing its molecular framework including a methoxy group, amino groups, and multiple hydroxyl groups in a sugar ring attached to a purine base.*
FDA Label Image

Nelarabine-single-carton (Single Carton)

Nelarabine-single-carton (Single Carton)
Nelarabine Injection 250 mg/50 mL (5 mg/mL) intravenous infusion, presented as a 50 mL single-dose vial. The label includes dosage form and strength, usage instructions indicating for intravenous infusion only, storage conditions, and a warning to discard unused portions. Labeler is XGen Pharmaceuticals DJB, Inc., with NDC 39822-0650-1.*

* 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.