药品名称PROLIXIN DECANOATE
申请号016727产品号001
活性成分FLUPHENAZINE DECANOATE市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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BRISTOL MYERS SQUIBB CO
化学类型New active ingredient审评分类Standard review drug
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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
016727053AP2002/10/04Manufacturing Change or Addition
016727052AP2001/09/17Manufacturing Change or Addition
016727051AP1994/08/16Package Change
016727050AP1994/08/11Control Supplement
016727049AP1996/02/15Manufacturing Change or Addition
016727048AP1991/03/26Package Change
016727043AP1987/06/15Manufacturing Change or Addition
016727042AP1987/06/15Package Change
016727039AP1986/09/19Manufacturing Change or Addition
016727037AP1985/10/23Manufacturing Change or Addition
016727036AP1985/02/12Package Change
016727034AP1984/06/29Labeling Revision
016727032AP1984/05/11Package Change
016727031AP1984/12/21Control Supplement
016727030AP1985/05/30Manufacturing Change or Addition
016727029AP1983/05/03Package Change
016727028AP1982/08/04Labeling Revision
016727027AP1982/08/04Labeling Revision
016727026AP1982/02/04Formulation Revision
016727024AP1981/09/10Control Supplement
016727022AP1981/04/16Package Change
016727021AP1981/03/23Manufacturing Change or Addition
016727020AP1981/01/09Labeling Revision
016727019AP1980/04/28Labeling Revision
016727017AP1979/12/20Labeling Revision
016727016AP1979/12/20Labeling Revision
016727015AP1980/01/04Control Supplement
016727010AP1979/02/06Labeling Revision
016727009AP1978/11/21Manufacturing Change or Addition
016727004AP1974/09/25Supplement
016727000AP1972/06/20Approval