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 |
018239 | 029 | AP | 2002/04/12 | Control Supplement |
018239 | 027 | AP | 2001/12/04 | Manufacturing Change or Addition |
018239 | 026 | AP | 2001/04/12 | Manufacturing Change or Addition |
018239 | 025 | AP | 2001/07/20 | Manufacturing Change or Addition |
018239 | 024 | AP | 2000/10/02 | Manufacturing Change or Addition |
018239 | 023 | AP | 2000/03/07 | Control Supplement |
018239 | 022 | AP | 1998/10/22 | Control Supplement |
018239 | 021 | AP | 1997/04/18 | Control Supplement |
018239 | 020 | AP | 1995/08/03 | Control Supplement |
018239 | 019 | AP | 1994/01/13 | Control Supplement |
018239 | 018 | AP | 1989/10/11 | Control Supplement |
018239 | 017 | AP | 1989/10/23 | Labeling Revision |
018239 | 016 | AP | 1989/10/23 | Package Change |
018239 | 014 | AP | 1988/02/09 | Labeling Revision |
018239 | 013 | AP | 1987/05/14 | Control Supplement |
018239 | 012 | AP | 1986/10/16 | Control Supplement |
018239 | 009 | AP | 1983/12/02 | Labeling Revision |
018239 | 007 | AP | 1982/08/13 | Control Supplement |
018239 | 006 | AP | 1987/04/09 | Final Printed Labeling - MarkIV |
018239 | 005 | AP | 1987/08/12 | Manufacturing Change or Addition |
018239 | 004 | AP | 1980/10/22 | Manufacturing Change or Addition |
018239 | 003 | AP | 1982/09/02 | Manufacturing Change or Addition |
018239 | 002 | AP | 1982/09/02 | Manufacturing Change or Addition |
018239 | 001 | AP | 1980/06/05 | Labeling Revision |
018239 | 000 | AP | 1980/05/02 | Approval |