Topotecan Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-762

5 FDA label images from Fresenius Kabi Usa, Llc · 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 Topotecan Hydrochloride (NDC 63323-762). 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.

Product Images & Figures Index

FDA Label Image

Top0e 0003 01

Top0e 0003 01
Chemical structure of Topotecan Hydrochloride showing its molecular configuration including rings, functional groups, and the associated hydrochloride molecule (1.25HCl).*
FDA Label Image

Top0e 0003 02

Top0e 0003 02
A survival curve chart comparing 'Topotecan plus Cisplatin' versus 'Cisplatin Monotherapy.' The y-axis represents the proportion surviving, from 0 to 1.0, and the x-axis shows months on study, ranging from 0 to 40. The graph includes a table of numbers at risk for each group at various time points.*
FDA Label Image

Top0e 0003 03

Top0e 0003 03
FDA Label Image

Top0e 0003 04

Top0e 0003 04
Topotecan Hydrochloride for Injection 4 mg per vial label by Fresenius Kabi USA, LLC. The label specifies that each vial contains topotecan hydrochloride equivalent to 4 mg topotecan base, includes inactive ingredients, and instructions for storage at 20 to 25°C. It is for intravenous use, must be diluted, and is a single-dose vial. The label includes handling cautions for this cytotoxic agent and a barcode with NDC 63323-762-10.*
FDA Label Image

Top0e 0003 05

Top0e 0003 05
Label for Topotecan Hydrochloride for Injection, 4 mg (base) per vial, by Fresenius Kabi USA, LLC. The label indicates the product is for intravenous use, must be diluted, and is a cytotoxic agent. It is a single-dose vial labeled Rx only.*

* 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.