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 |
010210 | 023 | AP | 1999/10/01 | Control Supplement |
010210 | 022 | AP | 1997/08/21 | Control Supplement |
010210 | 021 | AP | 1997/06/26 | Package Change |
010210 | 020 | AP | 1996/11/13 | Manufacturing Change or Addition |
010210 | 019 | AP | 1994/12/30 | Labeling Revision |
010210 | 018 | AP | 1989/04/06 | Package Change |
010210 | 017 | AP | 1989/01/03 | Manufacturing Change or Addition |
010210 | 016 | AP | 1987/05/12 | Manufacturing Change or Addition |
010210 | 015 | AP | 1987/03/16 | Control Supplement |
010210 | 014 | AP | 1986/05/20 | Control Supplement |
010210 | 013 | AP | 1986/04/28 | Manufacturing Change or Addition |
010210 | 012 | AP | 1986/04/28 | Manufacturing Change or Addition |
010210 | 011 | AP | 1986/03/11 | Manufacturing Change or Addition |
010210 | 010 | AP | 1984/09/09 | Labeling Revision |
010210 | 009 | AP | 1984/09/09 | Labeling Revision |
010210 | 008 | AP | 1988/03/23 | Practioner Draft Labeling |
010210 | 007 | AP | 1988/03/23 | Practioner Draft Labeling |
010210 | 006 | AP | 1988/03/23 | Labeling Revision |
010210 | 000 | AP | 1965/06/23 | Approval |