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 |
019787 | 059 | AP | 2015/03/23 | Labeling Revision |
019787 | 058 | AP | 2014/07/28 | Manufacturing Change or Addition |
019787 | 057 | AP | 2013/07/24 | Manufacturing Change or Addition |
019787 | 056 | AP | 2013/09/12 | Manufacturing Change or Addition |
019787 | 055 | AP | 2012/11/16 | Manufacturing Change or Addition |
019787 | 054 | AP | 2013/01/07 | Labeling Revision |
019787 | 053 | AP | 2013/01/07 | Labeling Revision |
019787 | 052 | AP | 2011/10/31 | Labeling Revision |
019787 | 047 | AP | 2011/05/09 | Labeling Revision |
019787 | 045 | AP | 2010/02/17 | Labeling Revision |
019787 | 042 | AP | 2007/10/31 | Labeling Revision |
019787 | 038 | AP | 2005/09/28 | New or Modified Indication |
019787 | 037 | AP | 2005/07/13 | Labeling Revision |
019787 | 032 | AP | 2002/05/28 | Labeling Revision |
019787 | 031 | AP | 2003/08/20 | Labeling Revision |
019787 | 030 | AP | 2004/01/08 | Patient Population Altered |
019787 | 029 | AP | 2001/08/13 | Manufacturing Change or Addition |
019787 | 028 | AP | 2001/08/10 | Manufacturing Change or Addition |
019787 | 027 | AP | 2003/12/03 | Labeling Revision |
019787 | 025 | AP | 2000/02/23 | Manufacturing Change or Addition |
019787 | 024 | AP | 2000/09/06 | Control Supplement |
019787 | 023 | AP | 2000/03/14 | Labeling Revision |
019787 | 022 | AP | 1999/12/15 | Control Supplement |
019787 | 021 | AP | 2000/02/01 | Package Change |
019787 | 020 | AP | 2000/07/12 | Efficacy Supplement with Clinical Data to Support |
019787 | 019 | AP | 1999/09/07 | Manufacturing Change or Addition |
019787 | 018 | AP | 1999/06/04 | Manufacturing Change or Addition |
019787 | 017 | AP | 2000/07/12 | Labeling Revision |
019787 | 016 | AP | 1998/03/09 | Control Supplement |
019787 | 015 | AP | 1997/05/16 | Manufacturing Change or Addition |
019787 | 014 | AP | 1997/04/18 | Control Supplement |
019787 | 013 | AP | 1997/01/08 | Labeling Revision |
019787 | 012 | AP | 1996/06/28 | Control Supplement |
019787 | 011 | AP | 1996/02/07 | Manufacturing Change or Addition |
019787 | 010 | AP | 1996/02/08 | Manufacturing Change or Addition |
019787 | 009 | AP | 1995/12/05 | Labeling Revision |
019787 | 008 | AP | 1995/11/02 | Control Supplement |
019787 | 007 | AP | 1996/06/14 | Patient Population Altered |
019787 | 006 | AP | 1995/06/19 | Control Supplement |
019787 | 005 | AP | 1995/02/07 | Manufacturing Change or Addition |
019787 | 004 | AP | 1994/05/03 | Control Supplement |
019787 | 003 | AP | 1994/03/03 | Control Supplement |
019787 | 002 | AP | 1995/01/12 | Labeling Revision |
019787 | 000 | AP | 1992/07/31 | Approval |