药品名称NEODECADRON
申请号050324产品号001
活性成分DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE市场状态停止上市
剂型或给药途径OINTMENT;OPHTHALMIC规格EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构MERCK AND CO 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
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
050324032AP1996/04/16Manufacturing Change or Addition
050324031AP1995/06/12Control Supplement
050324030AP1984/09/06Manufacturing Change or Addition
050324029AP1982/07/20Labeling Revision
050324028AP1981/10/13Labeling Revision
050324027AP1981/09/29Control Supplement
050324025AP1981/09/29Manufacturing Change or Addition
050324024AP1981/01/13Labeling Revision
050324023AP1980/08/28Labeling Revision
050324022AP1980/04/01Control Supplement
050324021AP1978/02/17Control Supplement
050324020AP1978/01/27New or Modified Indication
050324019AP1977/03/23Labeling Revision
050324018AP1976/02/23Control Supplement
050324017AP1976/01/09New or Modified Indication
050324016AP1975/03/07Formulation Revision
050324015AP1973/12/18Labeling Revision
050324014AP1972/09/07Labeling Revision
050324013AP1972/08/31Package Change
050324012AP1995/11/20Labeling Revision
050324011AP1995/11/20Labeling Revision
050324010AP1992/03/11Manufacturing Change or Addition
050324009AP1995/11/20Labeling Revision
050324008AP1995/11/20Labeling Revision
050324007AP1987/12/15Manufacturing Change or Addition
050324006AP1970/04/30Labeling Revision
050324005AP1969/12/24Control Supplement
050324004AP1984/09/06Control Supplement
050324003AP1984/07/10Labeling Revision
050324002AP1969/11/03Labeling Revision
050324001AP1984/02/28Manufacturing Change or Addition
050324000AP1969/09/15Approval