| 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 |
| 017243 | 046 | AP | 2015/05/04 | Labeling Revision |
| 017243 | 045 | AP | 2015/02/16 | Manufacturing Change or Addition |
| 017243 | 044 | AP | 2013/12/20 | Labeling Revision |
| 017243 | 043 | AP | 2014/02/18 | Labeling Revision |
| 017243 | 041 | AP | 2013/11/18 | Manufacturing Change or Addition |
| 017243 | 040 | AP | 2013/06/11 | Manufacturing Change or Addition |
| 017243 | 039 | AP | 2013/03/15 | Manufacturing Change or Addition |
| 017243 | 038 | AP | 2013/05/10 | Manufacturing Change or Addition |
| 017243 | 037 | AP | 2013/05/13 | Manufacturing Change or Addition |
| 017243 | 036 | AP | 2013/06/21 | Manufacturing Change or Addition |
| 017243 | 028 | AP | 2006/03/27 | Labeling Revision |
| 017243 | 025 | AP | 2004/10/15 | Control Supplement |
| 017243 | 022 | AP | 2003/01/16 | Control Supplement |
| 017243 | 021 | AP | 2002/04/19 | Manufacturing Change or Addition |
| 017243 | 020 | AP | 2002/03/04 | Control Supplement |
| 017243 | 019 | AP | 1999/12/29 | Formulation Revision |
| 017243 | 018 | AP | 1999/04/14 | Control Supplement |
| 017243 | 017 | AP | 1998/11/20 | Manufacturing Change or Addition |
| 017243 | 016 | AP | 1998/02/18 | Labeling Revision |
| 017243 | 015 | AP | 1997/06/18 | Manufacturing Change or Addition |
| 017243 | 014 | AP | 1996/08/20 | Control Supplement |
| 017243 | 013 | AP | 1997/03/21 | Control Supplement |
| 017243 | 012 | AP | 1996/07/16 | Control Supplement |
| 017243 | 010 | AP | 1984/03/26 | Practioner Draft Labeling |
| 017243 | 009 | AP | 1982/06/30 | Package Change |
| 017243 | 008 | AP | 1982/05/07 | Control Supplement |
| 017243 | 006 | AP | 1979/07/24 | Package Change |
| 017243 | 005 | AP | 1977/08/23 | Manufacturing Change or Addition |
| 017243 | 004 | AP | 1977/07/27 | Manufacturing Change or Addition |
| 017243 | 003 | AP | 1976/10/08 | Package Change |
| 017243 | 000 | AP | 1973/11/23 | Approval |
