药品名称DIPROSONE
申请号017781产品号001
活性成分BETAMETHASONE DIPROPIONATE市场状态停止上市
剂型或给药途径LOTION;TOPICAL规格EQ 0.05% BASE
治疗等效代码参比药物
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 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
历史专利信息
与本品相关的市场独占权保护信息
独占权代码失效日期
历史市场独占权保护信息
与药品注册相关的信息
申请号修订号审批结论公开文档类型文档创建时间获取文档
017781022APLetter2001/10/03下载
017781022APLabel2001/10/03下载
017781022APReview2001/10/03下载
017781015APLetter2001/10/03下载
017781015APLabel2001/10/03下载
017781015APReview2001/10/03下载
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
017781023AP2001/05/11Control Supplement
017781022AP2001/10/03Patient Population Altered
017781021AP2000/09/07Package Change
017781020AP1999/05/14Control Supplement
017781019AP1998/06/15Control Supplement
017781018AP1998/07/31Control Supplement
017781017AP1998/06/15Control Supplement
017781016AP1997/11/21Formulation Revision
017781015AP2001/10/03Labeling Revision
017781014AP1995/08/08Package Change
017781013AP1990/08/01Control Supplement
017781012AP1989/04/06Package Change
017781011AP1986/05/20Control Supplement
017781010AP1984/06/29Control Supplement
017781009AP1982/12/02Final Printed Labeling - MarkIV
017781008AP1982/04/19Manufacturing Change or Addition
017781007AP1981/09/02Manufacturing Change or Addition
017781006AP1981/09/15Control Supplement
017781004AP1980/06/26Expiration Date Change
017781003AP1979/07/06Control Supplement
017781002AP1980/05/12Control Supplement
017781001AP1980/04/24Labeling Revision
017781000AP1977/02/01Approval