NDAINHALATIONGAS
Approved
Apr 2025
Lifecycle
Launch
Competitive Pressure
30/100
Clinical Trials
16
Data completeness
4/8 — Partial
CARBON DIOXIDE, USP (carbon dioxide) by Martin Pharmaceuticals is x-ray contrast activity [moa]. First approved in 2025.
Drug data last refreshed 13h ago · AI intelligence enriched 2d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Carbon Dioxide, USP is an inhaled gas product approved as a radiographic contrast agent for X-ray imaging procedures. It functions through X-ray contrast activity to enhance visualization during diagnostic imaging. This product represents a novel application of a common gas in medical diagnostics.
LAUNCH
Early-stage launch product with emerging commercial potential; team building and market establishment phase underway.
Mechanism of Action
X-Ray Contrast Activity
Pharmacologic Class:
Radiographic Contrast Agent
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (16)
A Study of the Efficacy and Safety of Extracorporeal Carbon Dioxide Removal Using PrismaLung+
Started Dec 2025
99 enrolled
Acute Respiratory Distress SyndromeAcute Kidney Injury
Extracorporeal Carbon Dioxide Removal Using PrismaLung in Reducing Ventilator Induced Lung Injury
Started Feb 2024
15 enrolled
ARDS, Human
Carbon Dioxide Investigation
Started Jan 2024
42 enrolled
IntubationTracheostomyLaryngeal Mask
Influence of Caffeine on Psychomotor Vigilance and Carbon Dioxide Tolerance During Graded Hypercapnia
Started Nov 2023
29 enrolled
Hypercapnia
RECELL to Promote Healing Following Carbon Dioxide (CO2) Laser Treatment in Cosmetic Patients
Started Mar 2023
1 enrolled
Carbon Dioxide LaserPhotoaging
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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.