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 |
020641 | 042 | AP | 2016/08/09 | Labeling Revision |
020641 | 041 | AP | 2016/02/12 | Manufacturing Change or Addition |
020641 | 040 | AP | 2015/12/30 | Labeling Revision |
020641 | 039 | AP | 2015/12/10 | Manufacturing Change or Addition |
020641 | 038 | AP | 2015/11/05 | Labeling Revision |
020641 | 037 | AP | 2015/10/21 | Manufacturing Change or Addition |
020641 | 036 | AP | 2015/04/16 | Manufacturing Change or Addition |
020641 | 035 | AP | 2014/05/15 | Manufacturing Change or Addition |
020641 | 033 | AP | 2013/04/16 | Manufacturing Change or Addition |
020641 | 032 | AP | 2013/02/28 | Manufacturing Change or Addition |
020641 | 030 | AP | 2012/11/20 | Manufacturing Change or Addition |
020641 | 025 | AP | 2008/07/25 | Labeling Revision |
020641 | 024 | AP | 2008/07/25 | Package Change |
020641 | 018 | AP | 2005/06/14 | Formulation Revision |
020641 | 017 | AP | 2004/10/27 | Control Supplement |
020641 | 016 | AP | 2004/07/15 | Package Change |
020641 | 012 | AP | 2002/12/09 | Package Change |
020641 | 011 | AP | 2003/11/19 | OTC Labeling |
020641 | 010 | AP | 2002/07/23 | Expiration Date Change |
020641 | 009 | AP | 2002/11/27 | OTC Labeling |
020641 | 007 | AP | 2000/12/04 | Patient Population Altered |
020641 | 006 | AP | 1999/01/07 | Formulation Revision |
020641 | 003 | AP | 1998/10/29 | Manufacturing Change or Addition |
020641 | 002 | AP | 1998/03/30 | Labeling Revision |
020641 | 001 | AP | 1998/01/23 | Manufacturing Change or Addition |
020641 | 000 | AP | 1996/10/10 | Approval |