onditions.
6.5 Nature and contents of container
Sachets consisting of layers of polyethylene terephtalate (PET), aluminium (Al) and polyethylene (PE).
Pack size: carton box containing 50 sachets.
6.6 Special precautions for disposal and other handling
No special requirements.
7. Marketing authorisation holder
Astellas Pharma Europe B.V.
Sylviusweg 62
2333 BE Leiden
Netherlands
8. Marketing authorisation number(s)
Modigraf 0.2 mg granules for oral suspension
EU/1/09/523/001
Modigraf 1 mg granules for oral suspension
EU/1/09/523/002
9. Date of first authorisation/renewal of the authorisation
Date of first authorisation: 15 May 2009
Date of latest renewal: 17 February 2014
10. Date of revision of the text
25 June 2015
Detailed information on this medicinal product is available on the website of the European Medicines Agency http://www.ema.europa.eu.
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