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 |
018859 | 032 | AP | 2016/01/06 | Manufacturing Change or Addition |
018859 | 031 | AP | 2014/06/27 | Manufacturing Change or Addition |
018859 | 026 | AP | 2000/02/28 | Manufacturing Change or Addition |
018859 | 025 | AP | 1998/03/26 | Manufacturing Change or Addition |
018859 | 024 | AP | 1994/09/26 | Labeling Revision |
018859 | 023 | AP | 1994/03/10 | Package Change |
018859 | 022 | AP | 1993/04/01 | Labeling Revision |
018859 | 021 | AP | 1993/07/12 | Manufacturing Change or Addition |
018859 | 017 | AP | 1990/06/06 | Labeling Revision |
018859 | 016 | AP | 1993/03/04 | Control Supplement |
018859 | 015 | AP | 1989/03/13 | Control Supplement |
018859 | 014 | AP | 1989/03/13 | Control Supplement |
018859 | 013 | AP | 1992/09/23 | Manufacturing Change or Addition |
018859 | 012 | AP | 1989/03/28 | Control Supplement |
018859 | 008 | AP | 1988/09/15 | Manufacturing Change or Addition |
018859 | 006 | AP | 1989/06/02 | Manufacturing Change or Addition |
018859 | 005 | AP | 1987/04/09 | Manufacturing Change or Addition |
018859 | 003 | AP | 1993/02/05 | Patient Population Altered |
018859 | 002 | AP | 1986/08/27 | Expiration Date Change |
018859 | 001 | AP | 1986/08/27 | Manufacturing Change or Addition |
018859 | 000 | AP | 1985/12/31 | Approval |