美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=VENTAVIS"
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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
VENTAVIS 021779 001 NDA ILOPROST SOLUTION;INHALATION 20MCG/2ML (10MCG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 2004/12/29 2004/12/29 ACTELION Discontinued
VENTAVIS 021779 002 NDA ILOPROST SOLUTION;INHALATION 10MCG/ML (10MCG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2004/12/29 2005/12/08 ACTELION Discontinued
VENTAVIS 021779 003 NDA ILOPROST SOLUTION;INHALATION 20MCG/ML (20MCG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 2004/12/29 2009/08/07 ACTELION Discontinued
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