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Molecule

Sevoflurane

General Anesthetic
Available on requestPain and anaesthesia
Presentations
4
Brands
3
Manufacturers
3
Available from stock
0

Sevoflurane is a general anesthetic indicated for induction and maintenance of general anesthesia in adult and pediatric patients for inpatient and outpatient surgery. It is available as inhalation solution. MedsAcross supplies Sevoflurane for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
General Anesthetic, General Anesthesia
ATC classification
N01AB08 Sevoflurane · Anaesthetics, subgroup N01A, subgroup N01AB
US FDA first approval
7 June 1995
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Inhalation
Dosage forms
Inhalation solution
Identifiers
UNII 38LVP0K73ARxCUI 36453CAS 28523-86-6DrugBank DB01236Q419394

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

ULTANE is indicated for induction and maintenance of general anesthesia in adult and pediatric patients for inpatient and outpatient surgery. ULTANE should be administered only by persons trained in the administration of general anesthesia. Facilities for maintenance of a patent airway, artificial ventilation, oxygen enrichment, and circulatory resuscitation must be immediately available. Since level of anesthesia may be altered rapidly, only vaporizers producing predictable concentrations of sevoflurane should be used.

Source: US FDA prescribing information

Dosing overview

The concentration of sevoflurane being delivered from a vaporizer should be known. This may be accomplished by using a vaporizer calibrated specifically for sevoflurane. The administration of general anesthesia must be individualized based on the patient's response. Replacement of Desiccated CO 2 Absorbents When a clinician suspects that the CO 2 absorbent may be desiccated, it should be replaced. The exothermic reaction that occurs with sevoflurane and CO 2 absorbents is increased when the CO 2 absorbent becomes desiccated, such as after an extended period of dry gas flow through the CO 2 absorbent canisters. Pre-anesthetic Medication No specific premedication is either indicated or contraindicated with sevoflurane. The decision as to whether or not to premedicate and the choice of premedication is left to the discretion of the anesthesiologist.

Source: US FDA prescribing information

Contraindications

Known or suspected genetic susceptibility to malignant hyperthermia. Known or suspected sensitivity to sevoflurane or to other halogenated inhalational anesthetics.

Source: US FDA prescribing information

Warnings and precautions

Risk of Renal Injury Although data from controlled clinical studies at low flow rates are limited, findings taken from patient and animal studies suggest that there is a potential for renal injury which is presumed due to Compound A. Animal and human studies demonstrate that sevoflurane administered for more than 2 MAC·hours and at fresh gas flow rates of < 2 L/min may be associated with proteinuria and glycosuria. While a level of Compound A exposure at which clinical nephrotoxicity might be expected to occur has not been established, it is prudent to consider all of the factors leading to Compound A exposure in humans, especially duration of exposure, fresh gas flow rate, and concentration of sevoflurane. During sevoflurane anesthesia the clinician should adjust inspired concentration and fresh gas flow rate to minimize exposure to Compound A.

Source: US FDA prescribing information

Side effects

Clinical Trials Experience Adverse events are derived from controlled clinical studies conducted in the United States, Canada, and Europe. The reference drugs were isoflurane, enflurane, and propofol in adults and halothane in pediatric patients. The studies were conducted using a variety of premedications, other anesthetics, and surgical procedures of varying length. Most adverse events reported were mild and transient, and may reflect the surgical procedures, patient characteristics (including disease) and/or medications administered. Of the 5182 patients enrolled in the clinical studies, 2906 were exposed to sevoflurane, including 118 adults and 507 pediatric patients who underwent mask induction. Each patient was counted once for each type of adverse event.

Source: US FDA prescribing information

Interactions

In clinical studies, no significant adverse reactions occurred with other drugs commonly used in the perioperative period, including central nervous system depressants, autonomic drugs, skeletal muscle relaxants, anti-infective agents, hormones and synthetic substitutes, blood derivatives, and cardiovascular drugs. Epinephrine Epinephrine administered with sevoflurane may increase the risk of ventricular arrhythmias. Monitor the electrocardiogram and blood pressure and ensure emergency medications to treat ventricular arrhythmias are readily available. Calcium antagonists Sevoflurane may lead to marked hypotension in patients treated with calcium antagonists. Blood pressure should be closely monitored and emergency medications to treat hypotension should be readily available when calcium antagonists are used concomitantly with sevoflurane.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

4 presentations of Sevoflurane, sorted by availability.

MedicineManufacturerRegisterAvailability
Sevoflurane 250 mL/250 mL inhalation solutionInhalationGeneric name—US FDAAvailable on request
Ultane 250 mL/250 mL inhalation solutionInhalationAbbVieUS FDAAvailable on request
Sevoflurane, (Volatile for Inhalation) 250 mL/250 mL inhalation solutionInhalationMullan PharmaceuticalUS FDAAvailable on request
Sojourn 1 mL/mL inhalation solutionInhalationPiramal Critical CareIndiaUS FDAAvailable on request

Brands by market

3 brand names across 1 markets.

Brand names by country

Manufacturers

Indian manufacturers are highlighted.

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 7 June 1995Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Sevoflurane available for export from India?

Yes, on request. MedsAcross lists 4 presentations of Sevoflurane and sources them for licensed hospitals, importers and physicians against valid import documents. Indian manufacturers include Piramal Critical Care.

What brand names does Sevoflurane have?

The catalogue lists 3 brand names for Sevoflurane, including Sevoflurane, (Volatile for Inhalation), Sojourn, Ultane.

Is Sevoflurane approved by the US FDA?

Yes. The US FDA first approved Sevoflurane on 7 June 1995, according to Drugs@FDA.

Does Sevoflurane need cold chain shipping?

No listed presentation of Sevoflurane is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Sevoflurane in?

Sevoflurane is classified under ATC code N01AB08 (Sevoflurane).

References

  1. Ultane prescribing information (AbbVie). U.S. National Library of Medicine, DailyMed. Retrieved 12 February 2025

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