Mitoxantrone Injection, Solution
Product Images NDC 63323-132

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 Mitoxantrone (NDC 63323-132). 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

Vial (402231e)

Vial (402231e)
Mitoxantrone Injection, USP 2 mg/mL solution for intravenous use in a 12.5 mL multiple dose vial. The label specifies a 25 mg per 12.5 mL concentration, sterile preparation, preservative-free, with storage instructions to keep refrigerated but not frozen. The labeler is Fresenius Kabi USA, LLC, with product NDC 63323-132.*
FDA Label Image

Pbox (62852e)

Pbox (62852e)
Label of Mitoxantrone Injection, USP (Concentrate) 25 mg per 12.5 mL vial (2 mg/mL) by Fresenius Kabi USA, LLC. The label states it is for intravenous infusion after dilution, preservative free, Rx only, and a multiple dose vial. It includes a note to dispense the enclosed Medication Guide to patients.*
FDA Label Image

Logo (Fk17 Address)

Logo (Fk17 Address)
Mitoxantrone Injection, 2 mg/mL vial label from Fresenius Kabi USA, LLC. The label includes the proprietary name Mitoxantrone, the generic name MITOXANTRONE HYDROCHLORIDE, and indicates it is for intravenous use. The vial is clear with a blue cap and contains solution for injection. The manufacturer address is Lake Zurich, IL.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Mitoxantrone Hydrochloride showing its molecular formula C22H28N4O6 with 2 HCl molecules and a molecular weight of 517.41.*

* 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.