药品名称HALDOL
申请号015921产品号004
活性成分HALOPERIDOL市场状态停止上市
剂型或给药途径TABLET;ORAL规格5MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构ORTHO MCNEIL PHARMACEUTICAL
化学类型New molecular entity (NME)审评分类Priority 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
015921076AP2002/04/17Labeling Revision
015921075AP2000/05/02Labeling Revision
015921072AP1996/05/10Manufacturing Change or Addition
015921071AP1998/04/23Control Supplement
015921068AP1995/01/30Manufacturing Change or Addition
015921067AP1994/06/29Control Supplement
015921065AP1990/04/06Manufacturing Change or Addition
015921062AP1988/10/04Manufacturing Change or Addition
015921061AP1988/02/17Expiration Date Change
015921059AP1987/10/16Manufacturing Change or Addition
015921053AP1986/10/22Package Change
015921048AP1986/02/06Package Change
015921047AP1985/04/30Package Change
015921046AP1985/04/30Manufacturing Change or Addition
015921040AP1983/03/18Package Change
015921039AP1983/03/18Package Change
015921038AP1983/03/18Package Change
015921037AP1983/03/11Labeling Revision
015921036AP1983/01/31Labeling Revision
015921035AP1982/09/08Labeling Revision
015921034AP1982/09/03Control Supplement
015921033AP1982/04/20Manufacturing Change or Addition
015921032AP1982/06/23Manufacturing Change or Addition
015921031AP1981/10/02Labeling Revision
015921029AP1981/01/23Labeling Revision
015921028AP1981/01/23Labeling Revision
015921027AP1980/03/07Package Change
015921026AP1982/02/02Manufacturing Change or Addition
015921025AP1979/07/06Labeling Revision
015921024AP1980/02/12Labeling Revision
015921023AP1977/12/12Manufacturing Change or Addition
015921021AP1978/02/13Labeling Revision
015921020AP1976/03/26Control Supplement
015921019AP1974/12/10Control Supplement
015921012AP1974/05/21Other Amendment
015921000AP1967/04/12Approval