The contents of a vial should be used immediately after piercing of the rubber stopper.

Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7. Marketing authorisation holder
 Merck Sharp & Dohme Limited

Hertford Road, Hoddesdon

Hertfordshire EN11 9BU

United Kingdom

8. Marketing authorisation number(s)
 Puregon 50 IU/0.5 ml solution for injection

EU/1/96/008/17

EU/1/96/008/18

EU/1/96/008/19

Puregon 100 IU/0.5 ml solution for injection

EU/1/96/008/23

EU/1/96/008/24

EU/1/96/008/25

9. Date of first authorisation/renewal of the authorisation
 Date of first authorisation: 03 May 1996

Date of latest renewal: 03 May 2006
10. Date of revision of the text
20 February 2014
 
11. Legal category
 Prescription Only Medicine

Detailed information on this product is available on the website of the European Medicines Agency http://www.ema.europa.eu