PRED MILD(PREDNISOLONE ACETATE) - 美国FDA药品数据库

药品名称	PRED MILD
申请号	017100	产品号	001
活性成分	PREDNISOLONE ACETATE	市场状态	处方药
剂型或给药途径	SUSPENSION/DROPS;OPHTHALMIC	规格	0.12%
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 dosage form	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
017100	038	AP	2002/04/12	Control Supplement
017100	037	AP	2001/12/04	Manufacturing Change or Addition
017100	035	AP	2001/09/19	Manufacturing Change or Addition
017100	034	AP	2001/04/12	Manufacturing Change or Addition
017100	033	AP	2000/10/02	Manufacturing Change or Addition
017100	032	AP	1998/05/08	Control Supplement
017100	031	AP	1997/09/30	Control Supplement
017100	030	AP	1996/12/05	Control Supplement
017100	029	AP	1996/03/25	Control Supplement
017100	028	AP	1995/08/03	Control Supplement
017100	027	AP	1993/03/04	Formulation Revision
017100	026	AP	1990/12/07	Manufacturing Change or Addition
017100	025	AP	1989/04/27	Manufacturing Change or Addition
017100	024	AP	1989/10/13	Manufacturing Change or Addition
017100	023	AP	1988/12/08	Control Supplement
017100	022	AP	1987/10/29	Labeling Revision
017100	021	AP	1988/01/27	Labeling Revision
017100	019	AP	1986/07/08	Control Supplement
017100	018	AP	1986/06/06	Control Supplement
017100	015	AP	1982/08/13	Control Supplement
017100	013	AP	1982/09/02	Manufacturing Change or Addition
017100	012	AP	1982/09/02	Manufacturing Change or Addition
017100	011	AP	1980/01/29	Manufacturing Change or Addition
017100	010	AP	1980/09/04	Control Supplement
017100	008	AP	1977/02/23	Labeling Revision
017100	007	AP	1977/02/23	Labeling Revision
017100	006	AP	1977/02/23	Control Supplement
017100	004	AP	1977/02/23	Control Supplement
017100	003	AP	1977/02/28	Labeling Revision
017100	000	AP	1972/11/10	Approval