Product information (English only)
This Product information reflects the opinion of the Committee for Medicinal Products for Human Use, adopted on 19 November 2009, and show the changes made. The individual language files will be updated once the formal decision from the European Commission has been issued, and this is expected shortly.
The multilingual information below has been approved by the European Commission. It corresponds to the Commission's decision of 11 November 2009.
English |
bălgarski |
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español |
čeština |
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dansk |
Deutsch |
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eesti keel |
elliniká |
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français |
italiano |
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latviešu valoda |
lietuvių kalba |
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magyar |
Malti |
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Nederlands |
polski |
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português |
română |
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slovenčina |
slovenščina |
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suomi |
svenskas |
