PARAFON FORTE DSC(CHLORZOXAZONE) - 美国FDA药品数据库

药品名称	PARAFON FORTE DSC
申请号	011529	产品号	002
活性成分	CHLORZOXAZONE	市场状态	停止上市
剂型或给药途径	TABLET;ORAL	规格	500MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons
治疗等效代码		参比药物	否
批准日期	1987/06/15	申请机构	JANSSEN RESEARCH AND DEVELOPMENT LLC
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
011529	053	AP	2000/12/01	Manufacturing Change or Addition
011529	052	AP	2000/07/27	Manufacturing Change or Addition
011529	051	AP	2000/06/13	Manufacturing Change or Addition
011529	050	AP	1996/03/04	Manufacturing Change or Addition
011529	049	AP	1994/12/19	Labeling Revision
011529	048	AP	2002/06/28	Labeling Revision
011529	047	AP	1993/01/28	Control Supplement
011529	046	AP	1991/12/16	Manufacturing Change or Addition
011529	045	AP	1992/09/28	Manufacturing Change or Addition
011529	044	AP	1989/12/18	Manufacturing Change or Addition
011529	041	AP	1992/06/10	Labeling Revision
011529	036	AP	1987/06/15	Formulation Revision
011529	032	AP	1986/08/25	Package Change
011529	029	AP	1985/07/15	Manufacturing Change or Addition
011529	028	AP	1986/02/20	Package Change
011529	027	AP	1984/05/29	Control Supplement
011529	026	AP	1983/07/27	Control Supplement
011529	025	AP	1983/06/16	Manufacturing Change or Addition
011529	023	AP	1983/03/29	Package Change
011529	022	AP	1983/03/29	Package Change
011529	021	AP	1983/03/29	Package Change
011529	017	AP	1981/10/27	Labeling Revision
011529	012	AP	1977/04/29	Formulation Revision
011529	011	AP	1976/08/23	Distributor
011529	000	AP	1958/08/15	Approval