美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ALUPENT"
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
ALUPENT 016402 001 NDA METAPROTERENOL SULFATE AEROSOL, METERED;INHALATION 0.65MG/INH No No 1973/07/31 Approved Prior to Jan 1, 1982 BOEHRINGER INGELHEIM Discontinued
ALUPENT 015874 001 NDA METAPROTERENOL SULFATE TABLET;ORAL 20MG No No 1974/05/13 Approved Prior to Jan 1, 1982 BOEHRINGER INGELHEIM Discontinued
ALUPENT 015874 002 NDA METAPROTERENOL SULFATE TABLET;ORAL 10MG No No 1974/05/13 Approved Prior to Jan 1, 1982 BOEHRINGER INGELHEIM Discontinued
ALUPENT 017571 001 NDA METAPROTERENOL SULFATE SYRUP;ORAL 10MG/5ML No No 1975/05/23 Approved Prior to Jan 1, 1982 BOEHRINGER INGELHEIM Discontinued
ALUPENT 017659 001 NDA METAPROTERENOL SULFATE SOLUTION;INHALATION 5% No No 1980/09/18 Approved Prior to Jan 1, 1982 BOEHRINGER INGELHEIM Discontinued
ALUPENT 018761 001 NDA METAPROTERENOL SULFATE SOLUTION;INHALATION 0.6% No No 1983/06/30 1983/06/30 BOEHRINGER INGELHEIM Discontinued
ALUPENT 018761 002 NDA METAPROTERENOL SULFATE SOLUTION;INHALATION 0.4% No No 1983/06/30 1986/10/10 BOEHRINGER INGELHEIM Discontinued
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