Resumen de decisiones de la Unión Europea sobre autorizaciones de comercialización de medicamentos de 1 October 2018 a 31 December 2019[Publicadas conforme al artículo 13 o al artículo 38 del Reglamento (CE) n.o 726/2004 del Parlamento Europeo y del Consejo]
Section | Serie C |
Issuing Organization | Parlamento Europeo y Consejo de la Unión Europea |
26.6.2020 ES Diario Oficial de la Unión Europea C 213/1
Fecha de la decisión Nombre del medicamento Titular de la autorización de comercialización N.o de entrada en el registro comunitario Fecha de notificación 29.10.2018 Eporatio ratiopharm GmbH Graf-Arco-Straße 3, 89079 Ulm, Deutschland EU/1/09/573 31.10.2018 29.10.2018 Viramune Boehringer Ingelheim International GmbH Binger Straße 173, 55216 Ingelheim am Rhein, Deutschland EU/1/97/055 31.10.2018 28.11.2018 Keppra UCB Pharma SA Allée de la Recherche 60, 1070 Bruxelles, Belgique/Researchdreef 60, 1070 Brussel, België EU/1/00/146 30.11.2018 28.11.2018 Pioglitazona Teva Teva B.V. Swensweg 5, 2031 GA Haarlem, Nederland EU/1/12/757 30.11.2018 28.11.2018 Pioglitazona Teva Pharma Teva B.V. Swensweg 5, 2031 GA Haarlem, Nederland EU/1/12/758 30.11.2018 28.11.2018 Spinraza Biogen Netherlands B.V. Prins Mauritslaan 13, 1171 LP Badhoevedorp, Nederland EU/1/17/1188 30.11.2018 20.12.2018 Vimizim BioMarin International Limited Shanbally, Ringaskiddy, County Cork, P43 R298, Ireland EU/1/14/914 24.1.2019 11.4.2019 Apidra Sanofi-Aventis Deutschland GmbH D-65926 Fráncfort am Main, Deutschland EU/1/04/285 16.4.2019 15.4.2019 Orencia Bristol-Myers Squibb Pharma EEIG Plaza 254, Blanchardstown Corporate Park 2, D15 T867, Dublin 15, Ireland EU/1/07/389 17.4.2019 6.6.2019 Glustin Takeda Pharma A/S Dybendal Alle 10, 2630 Taastrup, Danmark EU/1/00/151 11.6.2019 27.6.2019 Xeljanz...
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