Source: Health Products Regulatory Authority (IE) Revision Year: 2023 Publisher: Aspen Pharma Trading Limited, 3016 Lake Drive, Citywest Business Campus, Dublin 24, Ireland
Ultiva 1 mg Powder for Concentrate for Solution for Infusion.
Pharmaceutical Form |
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Powder for concentrate for solution for infusion. A white to off-white, lyophilised powder. |
1 vial contains 1 mg remifentanil (as remifentanil hydrochloride).
For a full list of excipients, see section 6.1.
Active Ingredient | Description | |
---|---|---|
Remifentanil |
Remifentanil is a selective mu-opioid agonist with a rapid onset and very short duration of action. The mu-opioid activity, of remifentanil, is antagonised by narcotic antagonists, such as naloxone. |
List of Excipients |
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Glycine |
Ultiva injection for intravenous use is available as a glass vial with rubber stopper and aluminium overseal:
1 mg Remifentanil lyophilised powder in 3 ml vials in cartons of 5.
Not all pack sizes may be marketed.
Aspen Pharma Trading Limited, 3016 Lake Drive, Citywest Business Campus, Dublin 24, Ireland
PA1691/032/001
Date of first authorisation: 27 May 1999
Date of last renewal: 27 May 2009
Drug | Countries | |
---|---|---|
ULTIVA | Austria, Brazil, Cyprus, Ecuador, Spain, Finland, France, Hong Kong, Ireland, Israel, Japan, Lithuania, Mexico, Netherlands, New Zealand, Poland, Singapore, Tunisia, Turkey, United Kingdom, United States, South Africa |
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