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 |
011860 | 031 | AP | 1998/04/15 | Control Supplement |
011860 | 030 | AP | 1998/05/29 | Control Supplement |
011860 | 029 | AP | 1997/03/04 | Control Supplement |
011860 | 028 | AP | 1997/02/20 | Control Supplement |
011860 | 027 | AP | 1997/01/30 | Control Supplement |
011860 | 026 | AP | 1996/04/16 | Manufacturing Change or Addition |
011860 | 025 | AP | 1995/04/25 | Package Change |
011860 | 024 | AP | 1993/12/22 | Labeling Revision |
011860 | 023 | AP | 1991/04/23 | Labeling Revision |
011860 | 022 | AP | 1988/01/13 | Manufacturing Change or Addition |
011860 | 020 | AP | 1986/02/25 | Manufacturing Change or Addition |
011860 | 019 | AP | 1986/02/12 | Manufacturing Change or Addition |
011860 | 018 | AP | 1984/12/06 | Manufacturing Change or Addition |
011860 | 017 | AP | 1984/06/14 | Control Supplement |
011860 | 016 | AP | 1981/10/27 | Manufacturing Change or Addition |
011860 | 015 | AP | 1981/10/13 | Control Supplement |
011860 | 014 | AP | 1987/05/06 | Practioner Draft Labeling |
011860 | 013 | AP | 1981/07/15 | Manufacturing Change or Addition |
011860 | 012 | AP | 1979/12/21 | Control Supplement |
011860 | 011 | AP | 1978/07/05 | Labeling Revision |
011860 | 010 | AP | 1976/04/21 | Control Supplement |
011860 | 008 | AP | 1978/06/22 | Labeling Revision |
011860 | 000 | AP | 1959/08/05 | Approval |