药品名称CLEOCIN HYDROCHLORIDE
申请号050162产品号002
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 150MG 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
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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
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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