This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Japan, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey.
The drug SUPRANE contains one active pharmaceutical ingredient (API):
1
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UNII
CRS35BZ94Q - DESFLURANE
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Desflurane is one of a family of halogenated methyl ethyl ethers, which are administered by inhalation, producing a dose-related temporary loss of consciousness and of pain sensations, suppression of voluntary motor activity, reduction of autonomic reflexes, and depression of respiration and the cardiovascular system. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| N01AB07 | Desflurane | N Nervous system → N01 Anesthetics → N01A Anesthetics, general → N01AB Halogenated hydrocarbons |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| CA | Health Products and Food Branch | 02227428 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 21.280-1-05-04 |
| EE | Ravimiamet | 1023758, 1825332 |
| ES | Centro de información online de medicamentos de la AEMPS | 60554 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 043632 |
| FR | Base de données publique des médicaments | 65421851 |
| HK | Department of Health Drug Office | 51461 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-368795278 |
| JP | 医薬品医療機器総合機構 | 1119703G1024 |
| MT | Medicines Authority | MA1277/04501 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 540M96 |
| NL | Z-Index G-Standaard | 15959708 |
| NL | Z-Index G-Standaard, PRK | 42471 |
| NZ | Medicines and Medical Devices Safety Authority | 7164 |
| PL | Rejestru Produktów Leczniczych | 100085708 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W69338001, W69338002 |
| SG | Health Sciences Authority | 08818P |
| TN | Direction de la Pharmacie et du Médicament | 16973021H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681413881398, 8681413881404 |
| US | FDA, National Drug Code | 10019-641, 10019-644, 10019-646, 52584-641 |
| ZA | Health Products Regulatory Authority | 31/2.1/0417 |
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