LOTRIMIN(CLOTRIMAZOLE) - 美国FDA药品数据库

药品名称	LOTRIMIN
申请号	017619	产品号	001
活性成分	CLOTRIMAZOLE	市场状态	停止上市
剂型或给药途径	CREAM;TOPICAL	规格	1%
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 PLOUGH HEALTHCARE PRODUCTS INC
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
017619	035	AP	2002/01/10	Control Supplement
017619	034	AP	2001/02/28	Control Supplement
017619	033	AP	2001/01/29	Control Supplement
017619	032	AP	1998/11/10	Package Change
017619	031	AP	1998/05/29	Control Supplement
017619	030	AP	1998/05/18	Control Supplement
017619	027	AP	1992/05/21	Manufacturing Change or Addition
017619	026	AP	1992/06/23	Control Supplement
017619	025	AP	1990/02/06	Control Supplement
017619	022	AP	1989/10/27	OTC Labeling
017619	021	AP	1987/10/29	Manufacturing Change or Addition
017619	020	AP	1987/06/18	Control Supplement
017619	019	AP	1986/09/12	Manufacturing Change or Addition
017619	018	AP	1986/05/20	Control Supplement
017619	017	AP	1986/04/23	Manufacturing Change or Addition
017619	016	AP	1985/05/20	Labeling Revision
017619	015	AP	1985/07/24	Package Change
017619	014	AP	1984/07/03	Labeling Revision
017619	013	AP	1984/07/03	Practioner Draft Labeling
017619	012	AP	1981/08/18	Control Supplement
017619	011	AP	1981/10/13	Control Supplement
017619	010	AP	1981/06/04	Control Supplement
017619	009	AP	1980/02/27	Distributor
017619	008	AP	1980/01/14	Labeling Revision
017619	007	AP	1978/05/18	Manufacturing Change or Addition
017619	006	AP	1978/01/16	Package Change
017619	005	AP	1977/09/15	Manufacturing Change or Addition
017619	004	AP	1977/08/09	Manufacturing Change or Addition
017619	003	AP	1977/04/13	Package Change
017619	002	AP	1976/09/16	Control Supplement
017619	001	AP	1975/05/22	Supplement
017619	000	AP	1975/03/18	Approval