Amidate

Active Ingredient(s): Etomidate
FDA Approved: * September 7, 1982
Pharm Company: * HOSPIRA
Category: Anesthetic

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



Amidate Overview

Etomidate[1] (USAN, INN, BAN) (marketed as Amidate) is a short-acting intravenous anaesthetic agent used for the induction of general anaesthesia and sedation[2] for short procedures such as reduction of dislocated joints, tracheal intubation, and cardioversion. It was developed at Janssen Pharmaceutica in 1964 and was introduced as an intravenous agent in 1972 in Europe and in 1983 in the United States.[3] Contents 1 Medical uses 1.1 Sedat...

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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/Etomidate

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Possible Dosages for this and Related Drugs:

Etomidate
  • Injection: 2mg/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Amidate: (6 results)

Sorted by National Drug Code
  • 0409-6695 Amidate 2 mg/ml Intravenous Injection, Solution by Hospira, Inc.
  • 0409-8060 Amidate 2 mg/ml Intravenous Injection, Solution by Hospira, Inc.
  • 0409-8061 Amidate 2 mg/ml Intravenous Injection, Solution by Hospira, Inc.
  • 0409-8062 Amidate 2 mg/ml Intravenous Injection, Solution by Hospira, Inc.
  • 52584-060 Amidate 2 mg/ml Intravenous Injection, Solution by General Injectables and Vaccines, Inc.
  • 52584-695 Amidate 2 mg/ml Intravenous Injection, Solution by General Injectables & Vaccines, Inc

Other drugs which contain Etomidate or a similar ingredient: (1 result)






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