Genosyl Gas
Product Images NDC 72385-001

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Genosyl (NDC 72385-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vero Biotech, 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 (Genosyl01v1)

Chemical structure diagram of nitric oxide, the active ingredient in GENOSYL. The structure shows a nitrogen atom double bonded to an oxygen atom, with dots representing lone electrons.*

FDA Label Image

Genosyl02v2

A line graph titled 'Methemoglobin Concentration - Time Profiles Neonates Inhaling 0, 5, 20 or 80 ppm Nitric Oxide gas' showing the percentage of methemoglobin on the y-axis and hours of nitric oxide gas administration on the x-axis. Four lines represent different nitric oxide gas concentrations (0, 5, 20, 80 ppm) inhaled by neonates, with corresponding sample sizes noted. The graph tracks changes in methemoglobin levels over 12 hours.*

FDA Label Image

Label (Genosyl04v1)

Label for GENOSYL (nitric oxide) inhalation gas, 800 PPM strength, intended for use with the GENOSYL Delivery System only. Label includes NDC 72385-001-01 and storage instructions to keep at 25°C (77°F) with permitted excursions between 15°C and 30°C. Manufactured by VERO BIOTECH, LLC, Atlanta, GA.*

FDA Label Image

Top Label (Genosyl05v1)

GENOSYL (nitric oxide) for inhalation label showing the product name, NDC 72385-001-01, placeholders for lot number, serial number, and expiration date. The label includes the manufacturer Vero Biotech, LLC, with address in Atlanta, GA.*

* 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.