ully expel the air from the syringe and adjust the dose to the 0.05 ml mark on the syringe. The syringe is ready for injection.
Note: Do not wipe the injection needle. Do not pull back on the plunger.
After injection, do not recap the needle or detach it from the syringe. Dispose of the used syringe together with the needle in a sharps disposal container or in accordance with local requirements.
7. Marketing authorisation holder
Novartis Europharm Limited
Wimblehurst Road
Horsham
West Sussex, RH12 5AB
United Kingdom
8. Marketing authorisation number(s)
EU/1/06/374/001
9. Date of first authorisation/renewal of the authorisation
Date of first authorisation: 22 January 2007
Date of latest renewal: 24 January 2012
10. Date of revision of the text
23 January 2014
Detailed information on this medicinal product is available on the website of the European Medicines Agency http://www.ema.europa.eu
|
