NDAINHALATIONGAS
Approved
Jul 2013
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
2/8 — Basic
Drug data last refreshed 10h ago · AI intelligence enriched 13h ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
OXYGEN, USP is a medicinal gas product administered via inhalation to patients requiring supplemental oxygen therapy. It is an essential therapeutic agent used across acute and chronic respiratory conditions to maintain adequate tissue oxygenation. As a utility gas with no specific mechanism of action, it functions as a physiological replacement therapy rather than a pharmacological intervention.
Peak
As a peak-stage commodity product with low competitive differentiation (30% competitive pressure), career growth is tied to operational efficiency, supply chain management, and cost optimization rather than market expansion.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Pulmonary Hypertension and Oxygen Saturation Targeting in Preterm Infants
Started Sep 2026
39 enrolled
Bronchopulmonary DysplasiaPulmonary Hypertension
Safety Study of Intravenous Hydrogen-Oxygen Ultrafine Bubbles in Adults
Started May 2026
50 enrolled
Healthy Volunteer
MolecuLight All-in-One Oxygenation Clinical Utility
Started Mar 2026
18 enrolled
Wounds
Endoscopic COlorectal Mucosal Evaluation of Oxygen Tension
Started Mar 2026
80 enrolled
Anastomotic Leak RectumAnastomotic Leak Large Intestine
Impact of Intraoperative Oxygenation Practices on Patient Outcomes
Started Dec 2025
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.