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 |
020235 | 061 | AP | 2015/04/21 | Labeling Revision |
020235 | 060 | AP | 2015/09/14 | Labeling Revision |
020235 | 057 | AP | 2014/08/18 | Labeling Revision |
020235 | 056 | AP | 2013/05/01 | Labeling Revision |
020235 | 055 | AP | 2013/05/01 | Labeling Revision |
020235 | 054 | AP | 2013/05/01 | Labeling Revision |
020235 | 050 | AP | 2011/08/10 | Labeling Revision |
020235 | 043 | AP | 2010/10/11 | Labeling Revision |
020235 | 041 | AP | 2009/04/23 | Labeling Revision |
020235 | 036 | AP | 2011/03/01 | Labeling Revision |
020235 | 035 | AP | 2006/05/03 | Labeling Revision |
020235 | 029 | AP | 2005/02/18 | Labeling Revision |
020235 | 026 | AP | 2002/12/19 | Control Supplement |
020235 | 024 | AP | 2002/10/24 | Manufacturing Change or Addition |
020235 | 023 | AP | 2002/08/15 | Efficacy Supplement with Clinical Data to Support |
020235 | 022 | AP | 2002/01/30 | Labeling Revision |
020235 | 021 | AP | 2002/01/18 | Control Supplement |
020235 | 020 | AP | 2001/02/08 | Manufacturing Change or Addition |
020235 | 019 | AP | 2001/02/08 | Manufacturing Change or Addition |
020235 | 018 | AP | 2001/01/18 | Manufacturing Change or Addition |
020235 | 017 | AP | 2000/08/16 | Manufacturing Change or Addition |
020235 | 016 | AP | 2000/07/21 | Control Supplement |
020235 | 015 | AP | 2000/10/12 | New or Modified Indication |
020235 | 014 | AP | 2000/05/15 | Manufacturing Change or Addition |
020235 | 011 | AP | 1998/09/29 | New Dosage Regimen |
020235 | 009 | AP | 1998/02/12 | Manufacturing Change or Addition |
020235 | 005 | AP | 1996/12/09 | Manufacturing Change or Addition |
020235 | 004 | AP | 1996/05/28 | Manufacturing Change or Addition |
020235 | 003 | AP | 1996/04/09 | Package Change |
020235 | 001 | AP | 1994/11/14 | Labeling Revision |
020235 | 000 | AP | 1993/12/30 | Approval |