Clofarabine Injection
Product Images NDC 72205-394

View Photos of 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 Clofarabine (NDC 72205-394). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novadoz 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

Clofarabine--inj-crtn-label (Clofarabine Inj Crtn Label)

Clofarabine--inj-crtn-label (Clofarabine  Inj Crtn Label)
Packaging label for Clofarabine Injection, 20 mg/20 mL (1 mg/mL) intravenous injection in a 20 mL single-dose vial. The label indicates the product is Rx only, sterile, contains no preservatives, and must be diluted prior to intravenous use. It is distributed by Novadoz Pharmaceuticals LLC and manufactured by MSN Laboratories Private Limited, India. Storage instructions and contact information are also included.*
FDA Label Image

Clofarabine -inj-vial-label (Clofarabine Inj Vial Label)

Clofarabine -inj-vial-label (Clofarabine  Inj Vial Label)
Label for Clofarabine Injection 20 mg/20 mL (1 mg/mL) single-dose vial, intravenous use. The 20 mL vial must be diluted prior to administration. Manufactured by MSN Laboratories Private Limited in India and distributed by Novadoz Pharmaceuticals LLC.*
FDA Label Image

Clofarabine-structure (Clofarabine Structure)

Clofarabine-structure (Clofarabine Structure)
Chemical structure of clofarabine, showing its molecular framework with labeled nitrogen (N), chlorine (Cl), oxygen (O), fluorine (F), and hydrogen (H) atoms as part of the compound's nucleoside analog structure.*

* 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.