Human medicines European public assessment report (EPAR): Olanzapine Glenmark Europe, olanzapine, Date of authorisation: 03/12/2009, Revision: 15, Status: Authorised

Human medicines European public assessment report (EPAR): Olanzapine Glenmark Europe, olanzapine, Date of authorisation: 03/12/2009, Revision: 15, Status: Authorised

Human medicines European public assessment report (EPAR): Olanzapine Glenmark, olanzapine, Date of authorisation: 03/12/2009, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Olanzapine Glenmark, olanzapine, Date of authorisation: 03/12/2009, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Elebrato Ellipta, fluticasone furoate,umeclidinium,vilanterol, Date of authorisation: 15/11/2017, Revision: 14, Status: Authorised

Human medicines European public assessment report (EPAR): Elebrato Ellipta, fluticasone furoate,umeclidinium,vilanterol, Date of authorisation: 15/11/2017, Revision: 14, Status: Authorised

Human medicines European public assessment report (EPAR): Trelegy Ellipta, fluticasone furoate,umeclidinium,vilanterol, Date of authorisation: 15/11/2017, Revision: 13, Status: Authorised

Human medicines European public assessment report (EPAR): Trelegy Ellipta, fluticasone furoate,umeclidinium,vilanterol, Date of authorisation: 15/11/2017, Revision: 13, Status: Authorised

Human medicines European public assessment report (EPAR): Remsima, infliximab, Date of authorisation: 10/09/2013, Revision: 48, Status: Authorised

Human medicines European public assessment report (EPAR): Remsima, infliximab, Date of authorisation: 10/09/2013, Revision: 48, Status: Authorised

Human medicines European public assessment report (EPAR): Genvoya, elvitegravir,cobicistat,emtricitabine,tenofovir alafenamide, Date of authorisation: 19/11/2015, Revision: 29, Status: Authorised

Human medicines European public assessment report (EPAR): Genvoya, elvitegravir,cobicistat,emtricitabine,tenofovir alafenamide, Date of authorisation: 19/11/2015, Revision: 29, Status: Authorised

Human medicines European public assessment report (EPAR): Ixiaro, Japanese encephalitis vaccine (inactivated, adsorbed), Date of authorisation: 31/03/2009, Revision: 18, Status: Authorised

Human medicines European public assessment report (EPAR): Ixiaro, Japanese encephalitis vaccine (inactivated, adsorbed), Date of authorisation: 31/03/2009, Revision: 18, Status: Authorised

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