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 |
017525 | 049 | AP | 1998/09/16 | Labeling Revision |
017525 | 048 | AP | 1997/01/28 | Control Supplement |
017525 | 047 | AP | 1996/03/25 | Manufacturing Change or Addition |
017525 | 046 | AP | 1995/02/27 | Package Change |
017525 | 043 | AP | 1991/12/16 | Manufacturing Change or Addition |
017525 | 042 | AP | 1994/06/29 | Control Supplement |
017525 | 041 | AP | 1994/03/29 | Manufacturing Change or Addition |
017525 | 040 | AP | 1990/07/25 | Manufacturing Change or Addition |
017525 | 038 | AP | 1989/07/18 | Manufacturing Change or Addition |
017525 | 037 | AP | 1989/04/28 | Manufacturing Change or Addition |
017525 | 033 | AP | 1987/02/03 | Control Supplement |
017525 | 031 | AP | 1986/05/02 | Manufacturing Change or Addition |
017525 | 029 | AP | 1985/05/14 | Manufacturing Change or Addition |
017525 | 024 | AP | 1983/10/17 | Control Supplement |
017525 | 023 | AP | 1982/09/13 | Manufacturing Change or Addition |
017525 | 022 | AP | 1983/04/19 | Expiration Date Change |
017525 | 021 | AP | 1983/03/10 | General Efficacy (MarkIV) |
017525 | 020 | AP | 1981/10/08 | Labeling Revision |
017525 | 019 | AP | 1981/10/08 | Labeling Revision |
017525 | 018 | AP | 1981/01/06 | Manufacturing Change or Addition |
017525 | 016 | AP | 1979/04/24 | Manufacturing Change or Addition |
017525 | 015 | AP | 1980/09/16 | Control Supplement |
017525 | 014 | AP | 1979/11/08 | Formulation Revision |
017525 | 013 | AP | 1978/06/08 | Formulation Revision |
017525 | 012 | AP | 1978/01/25 | Labeling Revision |
017525 | 011 | AP | 1978/06/08 | Formulation Revision |
017525 | 009 | AP | 1976/08/23 | Distributor |
017525 | 007 | AP | 1976/11/30 | Formulation Revision |
017525 | 005 | AP | 1976/05/04 | Control Supplement |
017525 | 004 | AP | 1976/05/04 | Control Supplement |
017525 | 003 | AP | 1976/05/04 | Control Supplement |
017525 | 002 | AP | 1977/06/03 | Control Supplement |
017525 | 000 | AP | 1975/02/25 | Approval |