NDAINHALATIONLIQUID
Approved
Jun 1995
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
2/8 — Basic
Drug data last refreshed 12h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ULTANE (sevoflurane) is a volatile general anesthetic administered by inhalation for induction and maintenance of anesthesia in surgical and procedural settings. It is a small-molecule, non-halogenated ether that works as a central nervous system depressant to produce unconsciousness and analgesia. The drug is used across diverse patient populations requiring general anesthesia.
LOE Approaching
As LOE approaches, the brand team is likely consolidating around core maintenance and market defense with limited growth headroom; expect a compact, focused commercial organization.
Mechanism of Action
Pharmacologic Class:
General Anesthetic
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patients
Started May 2026
50 enrolled
AnesthesiaPediatric AnesthesiaTotal Intravenous Anesthesia
Does Boredom With Simultaneously Perceived Pain Affect Pressure Pain Thresholds
Started Jan 2026
161 enrolled
Pain Thresholds
Sevoflurane Sedation in Patients With Septic Shock
Started Jan 2026
Simultaneous Boost in Neoadjuvant Radiotherapy for Rectal Cancer
Started Oct 2025
156 enrolled
Locally Advanced Rectal Adenocarcinoma
Assessment of Hard and Soft Tissue Changes Following XCM Versus FGG Simultaneous With Delayed Dental Implant Placement
Started Sep 2025
24 enrolled
Missing Teeth
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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.