美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=OMONTYS"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
OMONTYS PRESERVATIVE FREE 202799 001 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 1MG BASE/0.5ML (EQ 1MG BASE/0.5ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS PRESERVATIVE FREE 202799 002 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 2MG BASE/0.5ML (EQ 2MG BASE/0.5ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS PRESERVATIVE FREE 202799 003 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 3MG BASE/0.5ML (EQ 3MG BASE/0.5ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS PRESERVATIVE FREE 202799 004 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 4MG BASE/0.5ML (EQ 4MG BASE/0.5ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS PRESERVATIVE FREE 202799 005 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 5MG BASE/0.5ML (EQ 5MG BASE/0.5ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS PRESERVATIVE FREE 202799 006 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 6MG BASE/0.5ML (EQ 6MG BASE/0.5ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS 202799 007 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 10MG BASE/ML (EQ 10MG BASE/ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
OMONTYS 202799 008 NDA PEGINESATIDE ACETATE SOLUTION;INTRAVENOUS, SUBCUTANEOUS EQ 20MG BASE/2ML (EQ 10MG BASE/ML) No No 2012/03/27 2012/03/27 TAKEDA PHARMS USA Discontinued
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