Xofluza Tablet, Film Coated
Product Images NDC 50242-877

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Xofluza (NDC 50242-877). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genentech, 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 (Xofluza 01)

Chemical structure of Baloxavir Marboxil, the active ingredient in Xofluza. The diagram shows the molecular arrangement of atoms including fluorine, sulfur, oxygen, nitrogen, and carbon components characteristic to this antiviral compound.*

FDA Label Image

Chemical Structure (Xofluza 02)

FDA Label Image

Chemical Structure (Xofluza 03)

Xofluza (baloxavir marboxil) oral suspension label for the 40 mg/20 mL (2 mg/mL) strength. The label indicates it is a granular oral suspension with instructions on dosing as a single one-time dose, measuring device use, and storage. The product is labeled by Genentech, Inc.*

FDA Label Image

Principal Display Panel (2x20 mg tablets (40 mg single dose))

Label for Xofluza (baloxavir marboxil) 40 mg tablet. The label specifies a total dose of 40 mg per tablet and includes instructions stating to take the tablet as a single, one-time dose. The label also displays the NDC number 50242-860-01 and the manufacturer labeler Genentech.*

FDA Label Image

Principal Display Panel (2x40 mg tablets (80 mg single dose))

Label for Xofluza (baloxavir marboxil) 80 mg tablet. The label indicates the total dose is one 80 mg tablet and provides usual dosage instructions for a single, one-time dose. The label also features the Genentech logo and NDC 50242-877-01.*

* 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.