VANCERIL(BECLOMETHASONE DIPROPIONATE) - 美国FDA药品数据库

药品名称	VANCERIL
申请号	017573	产品号	001
活性成分	BECLOMETHASONE DIPROPIONATE	市场状态	停止上市
剂型或给药途径	AEROSOL, METERED;INHALATION	规格	0.042MG/INH
治疗等效代码		参比药物	否
批准日期	Approved Prior to Jan 1, 1982	申请机构	SCHERING CORP SUB SCHERING PLOUGH CORP
化学类型	New molecular entity (NME)	审评分类	Priority review drug

与本品相关的专利信息（来自橙皮书Orange Book）
专利号	专利过期日	是否化合物专利	是否产品专利	专利用途代码	专利下载
无
历史专利信息
无

药品注册审批历史信息
申请号	修订号	审批结论	审批日期	审批内容
017573	045	AP	2000/08/30	Control Supplement
017573	044	AP	2000/07/26	Control Supplement
017573	041	AP	1999/03/11	Control Supplement
017573	040	AP	1999/02/08	Labeling Revision
017573	039	AP	1995/11/27	Control Supplement
017573	038	AP	1995/08/03	Control Supplement
017573	036	AP	1989/08/23	Labeling Revision
017573	034	AP	1988/08/02	Manufacturing Change or Addition
017573	031	AP	1987/09/24	Manufacturing Change or Addition
017573	030	AP	1988/02/01	Control Supplement
017573	029	AP	1986/07/08	Control Supplement
017573	028	AP	1986/03/06	Manufacturing Change or Addition
017573	027	AP	1986/02/24	Labeling Revision
017573	026	AP	1986/02/24	Control Supplement
017573	024	AP	1985/01/02	Control Supplement
017573	023	AP	1985/02/21	Control Supplement
017573	021	AP	1984/12/17	Control Supplement
017573	019	AP	1982/02/04	Control Supplement
017573	018	AP	1982/02/02	Control Supplement
017573	017	AP	1981/12/03	Control Supplement
017573	016	AP	1981/06/20	Control Supplement
017573	015	AP	1981/03/23	Control Supplement
017573	014	AP	1981/06/30	Labeling Revision
017573	013	AP	1981/01/13	Labeling Revision
017573	012	AP	1981/01/13	Manufacturing Change or Addition
017573	011	AP	1980/11/24	Labeling Revision
017573	009	AP	1980/06/23	Labeling Revision
017573	008	AP	1979/03/27	Distributor
017573	007	AP	1979/06/15	Control Supplement
017573	006	AP	1979/06/26	Control Supplement
017573	005	AP	1979/06/14	Labeling Revision
017573	004	AP	1979/04/06	Control Supplement
017573	003	AP	1979/04/13	Control Supplement
017573	002	AP	1979/06/14	Labeling Revision
017573	000	AP	1976/05/12	Approval