Cytarabine Injection, Solution
Product Images NDC 61703-305

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Cytarabine (NDC 61703-305). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Chemical Structure (Cytarabine 01)

FDA Label Image

Cytarabine 01a

Cytarabine 01a
Chemical structure of Cytarabine, showing its molecular formula C9H13N3O5 and molecular weight 243.22. The diagram illustrates the arrangement of atoms including nitrogen, oxygen, carbon, and hydrogen within the cytarabine molecule.*
FDA Label Image

Hospira Logo (Cytarabine 02)

FDA Label Image

Principal Display Panel (5 mL Vial Label)

Principal Display Panel (5 mL Vial Label)
Label for Cytarabine Injection 100 mg/5 mL (20 mg/mL) single dose vial by Hospira, Inc. The label indicates it is for intravenous, intrathecal, and subcutaneous use only and is preservative-free. It includes handling instructions, storage conditions of 20°C to 25°C (68°F to 77°F), and highlights that it is a cytotoxic agent.*
FDA Label Image

Principal Display Panel (5 mL Vial Carton)

Principal Display Panel (5 mL Vial Carton)
Packaging label for Cytarabine Injection 100 mg/5 mL (20 mg/mL) solution for injection in 5 x 5 mL single-dose vials. The label indicates use for intravenous, intrathecal, and subcutaneous routes and includes warnings that it is a cytotoxic agent. Labeler is Hospira, Inc., and storage instructions and inactive ingredients are noted on the label.*

* 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.