欧盟EMA药品数据库-欧盟集中审批药品
（European Medicines Agency Authorisation of Medicines DataBase）
请输入需要查询的英文药品名称，通用名称，活性成分，产品号
*Search by Medicine name,INN,Active substance,Product number.
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数据记录共 2679 条，共 134 页，当前第 70 页
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商品名称 适用类别 通用名称 活性成分 产品号 上市许可开发者/申请人/持有人 上市许可日期 许可状态
Olanzapine Glenmark Europe Human olanzapine olanzapine EMEA/H/C/001086 Glenmark Arzneimittel GmbH 2009/12/03 Authorised
Olanzapine Glenmark Human olanzapine olanzapine EMEA/H/C/001085 Glenmark Arzneimittel GmbH 2009/12/03 Authorised
Hirobriz Breezhaler Human indacaterol indacaterol maleate EMEA/H/C/001211 Novartis Europharm Limited 2009/11/30 Authorised
Zutectra Human human hepatitis B immunoglobulin human hepatitis B immunoglobulin EMEA/H/C/001089 Biotest Pharma GmbH 2009/11/30 Authorised
Nevirapine Teva Human nevirapine nevirapine EMEA/H/C/001119 Teva B.V.  2009/11/30 Withdrawn
Sildenafil Teva Human sildenafil sildenafil EMEA/H/C/001073 Teva B.V.  2009/11/30 Authorised
Oslif Breezhaler Human indacaterol indacaterol maleate EMEA/H/C/001210 Novartis Europharm Limited 2009/11/29 Authorised
Onbrez Breezhaler Human indacaterol indacaterol maleate EMEA/H/C/001114 Novartis Europharm Limited 2009/11/29 Authorised
Irbesartan/Hydrochlorothiazide Teva Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/001112 Teva B.V.  2009/11/26 Authorised
Multaq Human dronedarone dronedarone EMEA/H/C/001043 Sanofi Winthrop Industrie 2009/11/25 Authorised
Copalia HCT Human amlodipine;valsartan;hydrochlorothiazide amlodipine;valsartan;hydrochlorothiazide EMEA/H/C/001159 Novartis Europharm Limited 2009/11/03 Authorised
Dafiro HCT Human amlodipine besilate;valsartan;hydrochlorothiazide valsartan;hydrochlorothiazide;amlodipine besilate EMEA/H/C/001160 Novartis Europharm Limited 2009/11/03 Authorised
Repaglinide Krka Human repaglinide repaglinide EMEA/H/C/001066 Krka, d.d., Novo mesto 2009/11/03 Authorised
Irbesartan Teva Human irbesartan irbesartan EMEA/H/C/001093 Teva B.V. 2009/10/30 Authorised
Eporatio Human epoetin theta epoetin theta EMEA/H/C/001033 Ratiopharm GmbH 2009/10/29 Authorised
Ilaris Human canakinumab Canakinumab EMEA/H/C/001109 Novartis Europharm Limited 2009/10/23 Authorised
Lamivudine Teva Human lamivudine lamivudine EMEA/H/C/001113 Teva B.V. 2009/10/23 Authorised
Biopoin Human epoetin theta epoetin theta EMEA/H/C/001036 Teva GmbH 2009/10/23 Authorised
Rilonacept Regeneron (previously Arcalyst) Human rilonacept rilonacept EMEA/H/C/001047 Regeneron UK Limited 2009/10/23 Withdrawn
Foclivia Human pandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) influenza virus surface antigens, inactivated: A/Viet Nam/1194/2004 (H5N1) EMEA/H/C/001208 Seqirus S.r.l.  2009/10/18 Authorised

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