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 |
018141 | 029 | AP | 2007/09/05 | Labeling Revision |
018141 | 026 | AP | 2002/11/25 | Control Supplement |
018141 | 025 | AP | 2001/04/10 | Manufacturing Change or Addition |
018141 | 024 | AP | 2000/09/29 | Manufacturing Change or Addition |
018141 | 023 | AP | 1999/11/12 | Control Supplement |
018141 | 022 | AP | 1994/04/12 | Control Supplement |
018141 | 021 | AP | 1992/07/01 | Manufacturing Change or Addition |
018141 | 020 | AP | 1988/10/31 | Labeling Revision |
018141 | 019 | AP | 1989/02/17 | Control Supplement |
018141 | 017 | AP | 1989/01/12 | Manufacturing Change or Addition |
018141 | 016 | AP | 1989/01/12 | Manufacturing Change or Addition |
018141 | 013 | AP | 1985/01/30 | Control Supplement |
018141 | 011 | AP | 1986/04/23 | Manufacturing Change or Addition |
018141 | 009 | AP | 1985/05/09 | Practioner Draft Labeling |
018141 | 008 | AP | 1985/05/09 | Practioner Draft Labeling |
018141 | 007 | AP | 1985/05/09 | Manufacturing Change or Addition |
018141 | 006 | AP | 1980/11/06 | Manufacturing Change or Addition |
018141 | 005 | AP | 1981/02/09 | Distributor |
018141 | 004 | AP | 1982/03/31 | Manufacturing Change or Addition |
018141 | 003 | AP | 1980/06/09 | Distributor |
018141 | 001 | AP | 1989/06/12 | Package Change |
018141 | 000 | AP | 1979/06/26 | Approval |