药品名称DECADRON
申请号011984产品号001
活性成分DEXAMETHASONE SODIUM PHOSPHATE市场状态停止上市
剂型或给药途径SOLUTION/DROPS;OPHTHALMIC, OTIC规格EQ 0.1% PHOSPHATE
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
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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
011984046AP1997/07/31Control Supplement
011984045AP1997/08/29Control Supplement
011984044AP1997/03/04Control Supplement
011984043AP1996/12/02Control Supplement
011984042AP1996/04/16Manufacturing Change or Addition
011984041AP1995/04/25Package Change
011984040AP1994/12/22Control Supplement
011984039AP1994/10/21Labeling Revision
011984036AP1991/04/18Labeling Revision
011984035AP1988/02/16Manufacturing Change or Addition
011984034AP1988/10/17Labeling Revision
011984033AP1988/02/16Labeling Revision
011984031AP1986/02/25Manufacturing Change or Addition
011984030AP1988/10/17Labeling Revision
011984029AP1984/12/06Manufacturing Change or Addition
011984028AP1986/02/12Manufacturing Change or Addition
011984027AP1984/06/14Control Supplement
011984026AP1982/09/15Labeling Revision
011984025AP1988/02/16Practioner Draft Labeling
011984024AP1981/10/27Manufacturing Change or Addition
011984023AP1981/10/09Control Supplement
011984022AP1980/12/01Labeling Revision
011984021AP1981/07/15Manufacturing Change or Addition
011984020AP1982/05/14Manufacturing Change or Addition
011984019AP1980/09/17Control Supplement
011984018AP1980/05/28Labeling Revision
011984017AP1979/08/26Labeling Revision
011984016AP1980/01/08Labeling Revision
011984015AP1976/05/19Labeling Revision
011984014AP1976/04/21Control Supplement
011984000AP1959/09/02Approval