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 |
019785 | 021 | AP | 2016/10/20 | Manufacturing Change or Addition |
019785 | 018 | AP | 2008/04/30 | Patient Population Altered |
019785 | 015 | AP | 2000/06/08 | Control Supplement |
019785 | 014 | AP | 2000/02/11 | Manufacturing Change or Addition |
019785 | 013 | AP | 2000/01/14 | Labeling Revision |
019785 | 012 | AP | 2002/01/22 | Labeling Revision |
019785 | 011 | AP | 1998/06/10 | Control Supplement |
019785 | 010 | AP | 1997/08/08 | Manufacturing Change or Addition |
019785 | 009 | AP | 1997/04/24 | Manufacturing Change or Addition |
019785 | 008 | AP | 1996/09/26 | Manufacturing Change or Addition |
019785 | 007 | AP | 1996/11/08 | Control Supplement |
019785 | 006 | AP | 1997/05/23 | Patient Population Altered |
019785 | 005 | AP | 1995/12/14 | Patient Population Altered |
019785 | 004 | AP | 1995/12/14 | New or Modified Indication |
019785 | 003 | AP | 1996/02/28 | Control Supplement |
019785 | 002 | AP | 1992/09/09 | New or Modified Indication |
019785 | 001 | AP | 1992/01/30 | Manufacturing Change or Addition |
019785 | 000 | AP | 1990/12/21 | Approval |