Active Ingredient(s): Sevoflurane
FDA Approved: * June 7, 1995
Pharm Company: * ABBOTT
Category: Anesthetic

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Ultane Overview

Sevoflurane (1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)propane; synonym, fluoromethyl hexafluoroisopropyl ether), is a sweet-smelling, nonflammable, highly fluorinated methyl isopropyl ether used as an inhalational anaesthetic for induction and maintenance of general anesthesia. After desflurane, it is the volatile anesthetic with the fastest onset and offset.[1] It is one of the most commonly used volatile anesthetic agents, particularly for outpatient anesthesia,[2] across all ages, as well a...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Sevoflurane

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Possible Dosages for this and Related Drugs:

  • Liquid: 100%
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Ultane: (1 result)

Sorted by National Drug Code
  • 0074-4456 Ultane 250 ml/250ml Respiratory (Inhalation) Liquid by Abbvie Inc.

Other drugs which contain Sevoflurane or a similar ingredient: (2 results)