药品名称DELTASONE
申请号009986产品号008
活性成分PREDNISONE市场状态停止上市
剂型或给药途径TABLET;ORAL规格50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PHARMACIA AND UPJOHN CO
化学类型New formulation or new manufacturer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
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
009986056AP1993/05/24Manufacturing Change or Addition
009986055AP1993/12/28Labeling Revision
009986052AP1989/04/06Manufacturing Change or Addition
009986049AP1985/05/20Package Change
009986048AP1985/01/09Labeling Revision
009986045AP1979/07/23Manufacturing Change or Addition
009986044AP1979/04/25Control Supplement
009986043AP1979/01/17Control Supplement
009986042AP1978/10/18Labeling Revision
009986041AP1977/07/20Control Supplement
009986000AP1955/06/21Approval