欧盟EMA药品数据库-欧盟集中审批药品
(European Medicines Agency Authorisation of Medicines DataBase)
商品名称 适用类别 通用名称 活性成分 产品号 上市许可持有人/公司名称 上市批准日期 授权状态
Actelsar HCT Human telmisartan, hydrochlorothiazide Telmisartan, hydrochlorothiazide EMEA/H/C/002676 Actavis Group hf 2013/03/13 Authorised
Tolucombi Human telmisartan, hydrochlorothiazide Telmisartan, hydrochlorothiazide EMEA/H/C/002549 Krka, d.d., Novo mesto 2013/03/13 Authorised
Semintra Veterinary telmisartan Telmisartan EMEA/V/C/002436 Boehringer Ingelheim Vetmedica GmbH 2013/02/13 Authorised
Onduarp Human telmisartan, amlodipine Telmisartan EMEA/H/C/002118 Boehringer Ingelheim International GmbH 2011/11/24 Withdrawn
Telmisartan Teva Pharma Human telmisartan Telmisartan EMEA/H/C/002511 Teva B.V. 2011/10/03 Authorised
Twynsta Human telmisartan, amlodipine Telmisartan, amlodipine EMEA/H/C/001224 Boehringer Ingelheim International GmbH 2010/10/07 Authorised
Telmisartan Actavis Human telmisartan Telmisartan EMEA/H/C/001168 Actavis Group PTC ehf 2010/09/29 Authorised
Tolura Human telmisartan Telmisartan EMEA/H/C/001196 Krka, d.d., Novo mesto  2010/06/04 Authorised
Telmisartan Teva Human telmisartan Telmisartan EMEA/H/C/001146 Teva B.V. 2010/01/25 Withdrawn
PritorPlus Human telmisartan, hydrochlorothiazide Telmisartan, hydrochlorothiazide EMEA/H/C/000414 Bayer AG 2002/04/22 Authorised
MicardisPlus Human Telmisartan, hydrochlorothiazide EMEA/H/C/000413 Boehringer Ingelheim International GmbH 2002/04/19 Authorised
Kinzalkomb Human telmisartan, hydrochlorothiazide Telmisartan, hydrochlorothiazide EMEA/H/C/000415 Bayer AG 2002/04/19 Authorised
Kinzalmono (previously Telmisartan Boehringer Ingelheim Pharma KG) Human telmisartan Telmisartan EMEA/H/C/000211 Bayer AG 1998/12/16 Authorised
Micardis Human telmisartan Telmisartan EMEA/H/C/000209 Boehringer Ingelheim International GmbH 1998/12/16 Authorised
Pritor Human telmisartan Telmisartan EMEA/H/C/000210 Bayer AG 1998/12/11 Authorised

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