Cytarabine Injection, Solution
Product Images NDC 63323-120

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 Cytarabine (NDC 63323-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Cyt06 0001 01

Cyt06 0001 01
Chemical structure of Cytarabine, an active ingredient in injection, solution form. The diagram shows the molecular arrangement with nitrogen, oxygen, carbon, and hydrogen atoms, illustrating the compound's detailed chemical framework.*
FDA Label Image

Cyt06 0001 02

FDA Label Image

Cyt06 0001 03

Cyt06 0001 03
Cytarabine Injection 2 grams per 20 mL (100 mg/mL) single-dose vial label. The label states the solution is sterile, preservative-free, and for intravenous, intrathecal, and subcutaneous use. It contains 100 mg cytarabine per mL, with sodium hydroxide and/or hydrochloric acid to adjust pH. Storage instructions specify 20° to 25°C, protection from light, and not to refrigerate. Labeler is Fresenius Kabi USA, LLC.*
FDA Label Image

Cyt06 0001 04

Cyt06 0001 04
Carton label for Cytarabine Injection, 2 grams per 20 mL (100 mg/mL), a sterile injection solution by Fresenius Kabi USA, LLC. The label includes drug identity, strength, preservative-free status, routes of administration (intravenous, intrathecal, subcutaneous), storage instructions, and manufacturer information. It indicates the product is a single-dose 20 mL vial with the NDC 63323-120-20.*

* 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.