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 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
OXYGEN, USP is a gas-based therapeutic product administered via inhalation, approved by the FDA as a new drug application (NDA). While specific indications are not detailed in available data, oxygen therapy is a foundational respiratory treatment used across acute, chronic, and emergency care settings.
Peak
Peak lifecycle stage suggests stable market presence with moderate competitive intensity (30% competitive pressure); team size likely established with maintenance-focused operations.
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)
AI-Assisted Precision Hyperbaric Oxygen Therapy Based on Dynamic BIS-EEG Feedback for Patients With Disorders of Consciousness
Started Dec 2026
200 enrolled
Disorders of ConsciousnessVegetative StateMinimally Conscious State
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
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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.