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 |
020838 | 039 | AP | 2016/02/09 | Labeling Revision |
020838 | 038 | AP | 2013/04/26 | Labeling Revision |
020838 | 037 | AP | 2013/02/21 | Manufacturing Change or Addition |
020838 | 036 | AP | 2015/02/06 | Labeling Revision |
020838 | 035 | AP | 2012/04/27 | Labeling Revision |
020838 | 033 | AP | 2011/06/24 | Labeling Revision |
020838 | 032 | AP | 2012/04/13 | Labeling Revision |
020838 | 031 | AP | 2009/10/22 | Patient Population Altered |
020838 | 026 | AP | 2006/08/17 | Labeling Revision |
020838 | 024 | AP | 2005/02/22 | New or Modified Indication |
020838 | 023 | AP | 2004/12/16 | Labeling Revision |
020838 | 022 | AP | 2005/05/18 | New or Modified Indication |
020838 | 019 | AP | 2003/04/23 | Labeling Revision |
020838 | 017 | AP | 2003/01/22 | Labeling Revision |
020838 | 016 | AP | 2001/11/28 | Labeling Revision |
020838 | 015 | AP | 2002/09/13 | Comparative Efficacy Claim |
020838 | 014 | AP | 2001/10/04 | Control Supplement |
020838 | 013 | AP | 2001/03/29 | Package Change |
020838 | 012 | AP | 2001/05/24 | Manufacturing Change or Addition |
020838 | 011 | AP | 2001/04/02 | Manufacturing Change or Addition |
020838 | 010 | AP | 2001/06/07 | Manufacturing Change or Addition |
020838 | 009 | AP | 2000/12/27 | Manufacturing Change or Addition |
020838 | 008 | AP | 2000/06/14 | Labeling Revision |
020838 | 006 | AP | 1999/12/08 | Package Change |
020838 | 005 | AP | 1999/08/11 | Package Change |
020838 | 004 | AP | 1999/07/28 | Control Supplement |
020838 | 002 | AP | 1998/11/16 | Manufacturing Change or Addition |
020838 | 001 | AP | 1998/12/07 | Manufacturing Change or Addition |
020838 | 000 | AP | 1998/06/04 | Approval |