药品名称CLEOCIN HYDROCHLORIDE
申请号050162产品号001
活性成分CLINDAMYCIN HYDROCHLORIDE市场状态处方药
剂型或给药途径CAPSULE;ORAL规格EQ 75MG BASE
治疗等效代码AB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
050162097APLetter2016/08/03下载
050162097APLabel2016/08/09下载
050162096APLabel2016/03/29下载
050162096APLetter2016/03/25下载
050162095APLabel2016/03/29下载
050162095APLetter2016/03/25下载
050162093APLabel2014/06/30下载
050162093APLetter2014/06/27下载
050162092APLabel2014/06/30下载
050162092APLetter2014/06/27下载
050162090APLetter2011/06/10下载
050162085APLabel2009/11/23下载
050162085APLetter2010/01/21下载
050162084APLetter2004/02/02下载
050162082APLetter2004/10/04下载
050162082APLabel2004/10/04下载
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
050162097AP2016/08/02Labeling Revision
050162096AP2016/03/23Labeling Revision
050162095AP2016/03/23Labeling Revision
050162094AP2016/01/21Manufacturing Change or Addition
050162093AP2014/06/26Labeling Revision
050162092AP2014/06/26Labeling Revision
050162090AP2011/06/07Labeling Revision
050162085AP2009/11/20Labeling Revision
050162084AP2004/01/28Labeling Revision
050162083AP1999/11/15Package Change
050162082AP2004/09/29Labeling Revision
050162081AP1998/02/24Package Change
050162080AP1997/12/12Labeling Revision
050162079AP1997/07/17Labeling Revision
050162077AP1982/04/27Formulation Revision
050162076AP1981/11/03New Dosage Regimen
050162075AP1981/05/20Control Supplement
050162074AP1980/05/27Control Supplement
050162073AP1980/04/30Labeling Revision
050162072AP1979/11/06Labeling Revision
050162071AP1979/07/20Manufacturing Change or Addition
050162070AP1979/07/09Labeling Revision
050162069AP1979/07/09Labeling Revision
050162068AP1979/05/18Control Supplement
050162067AP1979/04/24Labeling Revision
050162066AP1978/10/04Labeling Revision
050162064AP1979/06/28Labeling Revision
050162063AP1978/07/11Labeling Revision
050162062AP1978/02/14Control Supplement
050162061AP1977/01/03Labeling Revision
050162060AP1976/07/02Control Supplement
050162059AP1976/06/02Control Supplement
050162058AP1976/01/28Control Supplement
050162057AP1977/08/15Labeling Revision
050162056AP1975/11/17Labeling Revision
050162055AP1975/06/11Labeling Revision
050162054AP1975/03/17Labeling Revision
050162053AP1975/03/14Labeling Revision
050162052AP1974/08/09Labeling Revision
050162051AP1974/06/06Control Supplement
050162050AP1974/08/16Labeling Revision
050162048AP1973/11/06Control Supplement
050162047AP1973/10/16Labeling Revision
050162046AP1973/07/20Package Change
050162045AP1974/04/24Labeling Revision
050162044AP1974/04/24Labeling Revision
050162043AP1973/04/03Labeling Revision
050162042AP1973/07/19Labeling Revision
050162041AP1973/01/12Control Supplement
050162040AP1972/07/25Labeling Revision
050162038AP1972/07/14Control Supplement
050162037AP1972/08/10Labeling Revision
050162036AP1972/05/11Control Supplement
050162034AP1972/04/12Labeling Revision
050162033AP1972/02/15Labeling Revision
050162032AP1972/05/22Expiration Date Change
050162029AP1971/09/22Labeling Revision
050162028AP1971/06/14Control Supplement
050162027AP1972/02/15Labeling Revision
050162024AP1971/07/22Labeling Revision
050162022AP1997/03/17Labeling Revision
050162021AP1993/03/05Manufacturing Change or Addition
050162020AP1995/02/21Labeling Revision
050162019AP1971/02/19Labeling Revision
050162018AP1997/03/17Labeling Revision
050162017AP1971/05/18Labeling Revision
050162016AP1970/12/18Labeling Revision
050162015AP1970/12/15Labeling Revision
050162014AP1970/12/09Labeling Revision
050162013AP1970/11/16Labeling Revision
050162012AP1971/04/26Labeling Revision
050162011AP1988/04/14New Dosage Regimen
050162010AP1986/10/20Labeling Revision
050162009AP1997/03/17Labeling Revision
050162007AP1985/06/21Labeling Revision
050162006AP1970/09/21Control Supplement
050162005AP1985/09/10Labeling Revision
050162004AP1983/04/29Package Change
050162003AP1970/07/01Control Supplement
050162001AP1970/05/22New or Modified Indication
050162000AP1970/02/22Approval