Floxuridine Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9270

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Floxuridine (NDC 0143-9270). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Floxuridine For Injection Usp 1)

Chemical structure diagram of floxuridine showing its molecular composition with a fluorine atom, nitrogen atoms, oxygen atoms, and hydroxyl groups arranged in the characteristic nucleoside structure.*

FDA Label Image

Floxuridine For Injection 500 mg/vial Label (Floxuridine For Injection Usp 2)

Floxuridine 500 mg/ vial injection, powder, lyophilized for solution for intra-arterial use only. The label indicates a 5 mL vial and provides directions for reconstitution and storage at 2° to 8°C. The product is labeled by Hikma Pharmaceuticals USA Inc. with NDC 0143-9270-01.*

FDA Label Image

Representative Carton Serialization Image (Floxuridine For Injection Usp 3)

The image shows a product label for Floxuridine injection, powder, lyophilized, for solution. It includes a 2D matrix barcode and printed information fields for lot number, expiration date, GTIN, and serial number in a black and white format. The label is consistent with a pharmaceutical container label for the 100 mg/mL strength by Hikma Pharmaceuticals USA Inc.*

* 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.