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 |
019452 | 024 | AP | 2007/12/12 | Patient Population Altered |
019452 | 020 | AP | 2005/11/09 | Efficacy Supplement with Clinical Data to Support |
019452 | 019 | AP | 2005/11/09 | Efficacy Supplement with Clinical Data to Support |
019452 | 018 | AP | 2003/04/21 | Package Change |
019452 | 017 | AP | 2001/10/10 | Patient Population Altered |
019452 | 016 | AP | 2005/11/09 | Efficacy Supplement with Clinical Data to Support |
019452 | 015 | AP | 1999/08/18 | New or Modified Indication |
019452 | 014 | AP | 1997/02/04 | Manufacturing Change or Addition |
019452 | 013 | AP | 1996/04/26 | Manufacturing Change or Addition |
019452 | 012 | AP | 1996/01/30 | Manufacturing Change or Addition |
019452 | 010 | AP | 1995/02/16 | New or Modified Indication |
019452 | 009 | AP | 1995/02/16 | Labeling Revision |
019452 | 008 | AP | 1992/06/25 | Package Change |
019452 | 007 | AP | 1996/08/27 | Control Supplement |
019452 | 005 | AP | 1990/10/16 | Manufacturing Change or Addition |
019452 | 004 | AP | 1990/01/10 | Manufacturing Change or Addition |
019452 | 003 | AP | 1989/06/27 | Manufacturing Change or Addition |
019452 | 002 | AP | 1989/03/15 | Manufacturing Change or Addition |
019452 | 001 | AP | 1988/09/08 | Manufacturing Change or Addition |
019452 | 000 | AP | 1988/02/03 | Approval |