药品名称PRED-G
申请号050586产品号001
活性成分GENTAMICIN SULFATE; PREDNISOLONE ACETATE市场状态处方药
剂型或给药途径SUSPENSION/DROPS;OPHTHALMIC规格EQ 0.3% BASE;1%
治疗等效代码参比药物
批准日期1988/06/10申请机构ALLERGAN PHARMACEUTICAL
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
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
050586026APLabel2006/01/05下载
050586026APLetter2006/01/19下载
050586025APLabel2006/01/05下载
050586025APLetter2006/01/19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
050586026AP2005/12/20Labeling Revision
050586025AP2005/12/20Package Change
050586024AP2002/04/12Control Supplement
050586023AP2001/12/04Manufacturing Change or Addition
050586021AP2001/09/28Manufacturing Change or Addition
050586020AP2001/04/12Manufacturing Change or Addition
050586019AP2000/10/02Manufacturing Change or Addition
050586018AP1999/04/26Manufacturing Change or Addition
050586017AP1998/05/08Control Supplement
050586016AP1997/10/01Control Supplement
050586015AP1996/12/02Control Supplement
050586014AP1995/08/03Control Supplement
050586013AP1991/12/30Labeling Revision
050586010AP1994/03/07Manufacturing Change or Addition
050586007AP1988/10/31Manufacturing Change or Addition
050586005AP1989/04/21New or Modified Indication
050586004AP1988/07/29Manufacturing Change or Addition
050586002AP1988/07/29Formulation Revision
050586001AP1988/11/30Labeling Revision
050586000AP1988/06/10Approval