欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Infanrix Penta
适用类别Human
治疗领域Hepatitis B;Tetanus;Immunization;Whooping Cough;Poliomyelitis;Diphtheria
通用名/非专利名称diphtheria (D), tetanus (T), pertussis (acellular, component) (Pa), hepatitis B (rDNA) (HBV), poliomyelitis (inactivated) (IPV) vaccine (adsorbed)
活性成分Diphtheria toxoid;tetanus toxoid;Bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin);poliovirus (inactivated) (type 1 (Mahoney strain), type 2 (MEF-1 strain), type 3 (Saukett strain));hepatitis B surface antigen
产品号EMEA/H/C/000295
患者安全信息No
许可状态Lapsed
ATC编码J07CA12
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2000/10/23
上市许可开发者/申请人/持有人GlaxoSmithKline Biologicals S.A.
人用药物治疗学分组Vaccines
兽用药物治疗学分组
欧盟委员会决定日期2010/08/31
修订号13
治疗适应症Infanrix Penta is indicated for primary and booster vaccination of infants against diphtheria, tetanus, pertussis, hepatitis B and poliomyelitis.
适用物种
兽用药物ATC编码
首次发布日期2010/08/31
最后更新日期2013/08/23
产品说明书https://www.ema.europa.eu/en/documents/product-information/infanrix-penta-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/infanrix-penta
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