药品名称MAXITROL
申请号050023产品号002
活性成分DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE市场状态处方药
剂型或给药途径SUSPENSION/DROPS;OPHTHALMIC规格0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
治疗等效代码AT参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ALCON LABORATORIES INC
化学类型审评分类
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
050023025APLetter2008/04/28下载
050023025APLabel2008/06/12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
050023031AP2015/05/27Manufacturing Change or Addition
050023025AP2008/04/24Labeling Revision
050023023AP2002/12/11Control Supplement
050023022AP2002/12/04Control Supplement
050023021AP2000/10/10Manufacturing Change or Addition
050023020AP2000/02/25Manufacturing Change or Addition
050023019AP1999/08/17Control Supplement
050023018AP1999/02/05Manufacturing Change or Addition
050023017AP1999/03/11Control Supplement
050023016AP1998/08/04Control Supplement
050023014AP1996/03/18Control Supplement
050023013AP1995/11/01Control Supplement
050023012AP1995/11/01Control Supplement
050023011AP1995/08/30Labeling Revision
050023010AP1994/07/27Control Supplement
050023009AP1993/01/22Manufacturing Change or Addition
050023008AP1995/06/13Package Change
050023006AP1989/03/03Control Supplement
050023005AP1977/03/25Control Supplement
050023004AP1976/03/01Control Supplement
050023003AP1973/02/20Control Supplement
050023002AP1971/10/14Control Supplement
050023001AP1966/12/14Expiration Date Change
050023000AP1963/06/06Approval