美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=FLOVENT"
符合检索条件的记录共 12 条
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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
FLOVENT 020548 001 NDA FLUTICASONE PROPIONATE AEROSOL, METERED;INHALATION 0.044MG/INH No No 1996/03/27 1996/03/27 GLAXOSMITHKLINE Discontinued
FLOVENT 020548 002 NDA FLUTICASONE PROPIONATE AEROSOL, METERED;INHALATION 0.11MG/INH No No 1996/03/27 1996/03/27 GLAXOSMITHKLINE Discontinued
FLOVENT 020548 003 NDA FLUTICASONE PROPIONATE AEROSOL, METERED;INHALATION 0.22MG/INH No No 1996/03/27 1996/03/27 GLAXOSMITHKLINE Discontinued
FLOVENT 020549 001 NDA FLUTICASONE PROPIONATE POWDER;INHALATION 0.044MG/INH No No 1997/11/07 1997/11/07 GLAXOSMITHKLINE Discontinued
FLOVENT 020549 002 NDA FLUTICASONE PROPIONATE POWDER;INHALATION 0.088MG/INH No No 1997/11/07 1997/11/07 GLAXOSMITHKLINE Discontinued
FLOVENT 020549 003 NDA FLUTICASONE PROPIONATE POWDER;INHALATION 0.22MG/INH No No 1997/11/07 1997/11/07 GLAXOSMITHKLINE Discontinued
FLOVENT DISKUS 50 020833 001 NDA FLUTICASONE PROPIONATE POWDER;INHALATION 0.05MG/INH Yes Yes 2000/09/29 2000/09/29 GLAXO GRP LTD Prescription
FLOVENT DISKUS 100 020833 002 NDA FLUTICASONE PROPIONATE POWDER;INHALATION 0.1MG/INH Yes Yes 2000/09/29 2000/09/29 GLAXO GRP LTD Prescription
FLOVENT DISKUS 250 020833 003 NDA FLUTICASONE PROPIONATE POWDER;INHALATION 0.25MG/INH Yes Yes 2000/09/29 2000/09/29 GLAXO GRP LTD Prescription
FLOVENT HFA 021433 001 NDA FLUTICASONE PROPIONATE AEROSOL, METERED;INHALATION 0.22MG/INH Yes Yes 2004/05/14 2004/05/14 GLAXO GRP LTD Prescription
FLOVENT HFA 021433 002 NDA FLUTICASONE PROPIONATE AEROSOL, METERED;INHALATION 0.11MG/INH Yes Yes 2004/05/14 2004/05/14 GLAXO GRP LTD Prescription
FLOVENT HFA 021433 003 NDA FLUTICASONE PROPIONATE AEROSOL, METERED;INHALATION 0.044MG/INH Yes Yes 2004/05/14 2004/05/14 GLAXO GRP LTD Prescription
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