美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PROVENTIL"
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
PROVENTIL 017559 001 NDA ALBUTEROL AEROSOL, METERED;INHALATION 0.09MG/INH No No 1981/05/01 Approved Prior to Jan 1, 1982 SCHERING Discontinued
PROVENTIL 017853 001 NDA ALBUTEROL SULFATE TABLET;ORAL EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1982/05/07 1982/05/07 SCHERING Discontinued
PROVENTIL 017853 002 NDA ALBUTEROL SULFATE TABLET;ORAL EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1982/05/07 1982/05/07 SCHERING Discontinued
PROVENTIL 018062 001 NDA ALBUTEROL SULFATE SYRUP;ORAL EQ 2MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1983/01/19 1983/01/19 SCHERING Discontinued
PROVENTIL 019243 001 NDA ALBUTEROL SULFATE SOLUTION;INHALATION EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1987/01/14 1987/01/14 SCHERING Discontinued
PROVENTIL 019243 002 NDA ALBUTEROL SULFATE SOLUTION;INHALATION EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1987/01/14 1987/01/14 SCHERING Discontinued
PROVENTIL 019383 001 NDA ALBUTEROL SULFATE TABLET, EXTENDED RELEASE;ORAL EQ 4MG BASE No No 1987/07/13 1987/07/13 SCHERING Discontinued
PROVENTIL-HFA 020503 001 NDA ALBUTEROL SULFATE AEROSOL, METERED;INHALATION EQ 0.09MG BASE/INH Yes Yes 1996/08/15 1996/08/15 3M DRUG DELIVERY Prescription
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