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 |
020372 | 025 | AP | 2013/03/08 | Manufacturing Change or Addition |
020372 | 022 | AP | 2009/02/26 | Formulation Revision |
020372 | 019 | AP | 2005/07/07 | Formulation Revision |
020372 | 015 | AP | 2003/11/13 | Labeling Revision |
020372 | 013 | AP | 2003/02/28 | New or Modified Indication |
020372 | 012 | AP | 2002/11/25 | Control Supplement |
020372 | 011 | AP | 2002/05/22 | Manufacturing Change or Addition |
020372 | 010 | AP | 2001/12/04 | Manufacturing Change or Addition |
020372 | 009 | AP | 2001/08/27 | Manufacturing Change or Addition |
020372 | 008 | AP | 2001/04/10 | Manufacturing Change or Addition |
020372 | 007 | AP | 2000/09/29 | Manufacturing Change or Addition |
020372 | 006 | AP | 2000/04/12 | Manufacturing Change or Addition |
020372 | 005 | AP | 2000/04/13 | Expiration Date Change |
020372 | 004 | AP | 1999/11/12 | Control Supplement |
020372 | 003 | AP | 2001/11/23 | New or Modified Indication |
020372 | 002 | AP | 1998/12/09 | Manufacturing Change or Addition |
020372 | 001 | AP | 1998/12/07 | Manufacturing Change or Addition |
020372 | 000 | AP | 1996/02/09 | Approval |