BLEPHAMIDE(PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM)

药品名称	BLEPHAMIDE
申请号	012813	产品号	002
活性成分	PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM	市场状态	处方药
剂型或给药途径	SUSPENSION;OPHTHALMIC	规格	0.2%;10%
治疗等效代码		参比药物	是
批准日期	Approved Prior to Jan 1, 1982	申请机构	ALLERGAN PHARMACEUTICAL
化学类型	New combination	审评分类	Standard 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
012813	054	AP	2002/04/12	Control Supplement
012813	053	AP	2001/12/04	Manufacturing Change or Addition
012813	052	AP	2001/04/12	Manufacturing Change or Addition
012813	051	AP	2001/03/26	Manufacturing Change or Addition
012813	050	AP	2000/10/02	Manufacturing Change or Addition
012813	049	AP	2000/04/21	Control Supplement
012813	048	AP	2000/04/21	Control Supplement
012813	047	AP	1999/12/03	Control Supplement
012813	046	AP	1998/01/09	Control Supplement
012813	045	AP	1998/05/21	Control Supplement
012813	044	AP	1997/09/30	Control Supplement
012813	043	AP	1998/08/03	Labeling Revision
012813	042	AP	1996/12/02	Expiration Date Change
012813	041	AP	1994/06/22	Control Supplement
012813	040	AP	1995/08/03	Control Supplement
012813	039	AP	1993/04/13	Manufacturing Change or Addition
012813	038	AP	1990/08/06	Manufacturing Change or Addition
012813	037	AP	1989/11/07	Manufacturing Change or Addition
012813	036	AP	1989/03/14	Control Supplement
012813	035	AP	1986/11/10	Manufacturing Change or Addition
012813	034	AP	1986/03/14	Control Supplement
012813	033	AP	1986/07/18	Control Supplement
012813	032	AP	1986/07/07	Manufacturing Change or Addition
012813	031	AP	1985/08/23	Control Supplement
012813	030	AP	1985/07/09	Expiration Date Change
012813	029	AP	1998/08/03	Package Change
012813	025	AP	1981/09/25	Formulation Revision
012813	024	AP	1982/09/15	Manufacturing Change or Addition
012813	023	AP	1982/09/15	Manufacturing Change or Addition
012813	021	AP	1980/05/08	Control Supplement
012813	020	AP	1978/11/07	Manufacturing Change or Addition
012813	000	AP	1961/09/18	Approval