美国FDA药品数据库-药物在线

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NDA	ALBUTEROL SULFATE	TABLET;ORAL	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1982/05/07	1982/05/07	SCHERING	Discontinued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NDA	ALBUTEROL SULFATE	TABLET;ORAL	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1982/05/07	1982/05/07	SCHERING	Discontinued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NDA	ALBUTEROL SULFATE	SYRUP;ORAL	EQ 2MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1983/01/19	1983/01/19	SCHERING	Discontinued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ALBUTEROL SULFATE	SOLUTION;INHALATION	EQ 0.5% BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/01/14	1987/01/14	SCHERING	Discontinued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SULFATE	SOLUTION;INHALATION	EQ 0.083% BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1987/01/14	1987/01/14	SCHERING	Discontinued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	KINDEVA	Prescription