Summary of opinion: Prevexxion RN+HVT,Marek’s disease virus, strain RN1250, live,Turkey herpesvirus, strain FC126, Live, 07/09/2023, Positive

Summary of opinion: Prevexxion RN+HVT,Marek’s disease virus, strain RN1250, live,Turkey herpesvirus, strain FC126, Live, 07/09/2023, Positive

Human medicines European public assessment report (EPAR): Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen), aripiprazole, Schizophrenia;Bipolar Disorder, Date of authorisation: 30/06/2015, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Aripiprazole Mylan Pharma (previously Aripiprazole Pharmathen), aripiprazole, Schizophrenia;Bipolar Disorder, Date of authorisation: 30/06/2015, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Dimethyl fumarate Mylan, dimethyl fumarate, Multiple Sclerosis, Relapsing-Remitting, Date of authorisation: 13/05/2022, Revision: 4, Status: Authorised

Human medicines European public assessment report (EPAR): Dimethyl fumarate Mylan, dimethyl fumarate, Multiple Sclerosis, Relapsing-Remitting, Date of authorisation: 13/05/2022, Revision: 4, Status: Authorised

Human medicines European public assessment report (EPAR): Natpar, parathyroid hormone, Hypoparathyroidism, Date of authorisation: 24/04/2017, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Natpar, parathyroid hormone, Hypoparathyroidism, Date of authorisation: 24/04/2017, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Akynzeo, netupitant,palonosetron, Vomiting;Neoplasms;Nausea;Cancer, Date of authorisation: 27/05/2015, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Akynzeo, netupitant,palonosetron, Vomiting;Neoplasms;Nausea;Cancer, Date of authorisation: 27/05/2015, Revision: 16, Status: Authorised

Flurbiprofen : CMDh Scientific conclusions and grounds for variation, amendments to the Product Information and timetable for the implementation - PSUSA/00001450/202211

Flurbiprofen : CMDh Scientific conclusions and grounds for variation, amendments to the Product Information and timetable for the implementation - PSUSA/00001450/202211

Human medicines European public assessment report (EPAR): Esbriet, pirfenidone, Idiopathic Pulmonary Fibrosis;Lung Diseases;Respiratory Tract Diseases, Date of authorisation: 27/02/2011, Revision: 33, Status: Authorised

Human medicines European public assessment report (EPAR): Esbriet, pirfenidone, Idiopathic Pulmonary Fibrosis;Lung Diseases;Respiratory Tract Diseases, Date of authorisation: 27/02/2011, Revision: 33, Status: Authorised

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