NDAINHALATIONGAS
Approved
Mar 2017
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
6
Data completeness
3/8 — Basic
Drug data last refreshed 10h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Nitrous Oxide, USP is an inhalational gas approved by the FDA in 2017 as a pharmaceutical product for medical use. It is a small-molecule inhalant with established anesthetic and analgesic properties. The drug is indicated for use in medical settings where rapid onset and offset of effect are clinically beneficial.
Peak
Product is in peak commercial stage with modest competitive pressure (30%), indicating stable market position and team size.
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 (6)
Nitrous Oxide Prior to Intranasal Midazolam for Moderate Dental Sedation in Pediatric Patients
Started Jul 2019
150 enrolled
Dental AnxietyPain
Nitrous Oxide For Endoscopic Ablation of Refractory Barrett's Esophagus (NO FEAR-BE)
Started Sep 2018
70 enrolled
Barrett EsophagusIntestinal MetaplasiaEsophageal Dysplasia
A Comparison of Intranasal Midazolam and Nitrous Oxide (N2O) Minimal Sedation for Minor Procedures in a Pediatric Emergency Department
Started May 2017
63 enrolled
Conscious SedationSimple Lacerations Less Than 4 cmLumbar Punctures+1 more
Nitrous Oxide Versus Intravenous Sedation for Anesthesia
Started Jul 2016
39 enrolled
Pregnancy Termination in Second Trimester
Nitrous Oxide for Pain Management During In-office Transcervical Sterilization
Started Feb 2014
72 enrolled
ContraceptionInhalation of Nitrous Oxide
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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.