NDAINHALATIONGAS
Approved
Jun 2013
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
2/8 — Basic
Drug data last refreshed 17h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
OXYGEN, USP is a pharmaceutical-grade oxygen gas administered via inhalation for patients with hypoxemia and respiratory insufficiency. As an essential therapeutic gas rather than a traditional small-molecule drug, it serves as foundational supportive care across acute and chronic respiratory conditions. Oxygen therapy works by increasing alveolar oxygen partial pressure to restore adequate tissue oxygenation.
Peak
Oxygen USP operates in a mature, non-differentiated commodity market with moderate competitive pressure (30); team focus is on distribution efficiency and clinical education 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)
Safety Study of Intravenous Hydrogen-Oxygen Ultrafine Bubbles in Adults
Started May 2026
50 enrolled
Healthy Volunteer
Pulmonary Hypertension and Oxygen Saturation Targeting in Preterm Infants
Started Apr 2026
39 enrolled
Bronchopulmonary DysplasiaPulmonary Hypertension
MolecuLight All-in-One Oxygenation Clinical Utility
Started Mar 2026
20 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.