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 |
018024 | 040 | AP | 2005/08/23 | Supplement |
018024 | 039 | AP | 2002/10/25 | Control Supplement |
018024 | 038 | AP | 2002/01/15 | Control Supplement |
018024 | 037 | AP | 2002/04/16 | Manufacturing Change or Addition |
018024 | 036 | AP | 2003/04/30 | Labeling Revision |
018024 | 035 | AP | 1995/12/15 | Control Supplement |
018024 | 033 | AP | 1993/10/15 | Control Supplement |
018024 | 032 | AP | 1994/11/02 | Labeling Revision |
018024 | 031 | AP | 1990/10/19 | Manufacturing Change or Addition |
018024 | 029 | AP | 1988/11/10 | Formulation Revision |
018024 | 028 | AP | 1987/12/07 | Control Supplement |
018024 | 027 | AP | 1988/11/10 | Labeling Revision |
018024 | 026 | AP | 1987/08/04 | Labeling Revision |
018024 | 024 | AP | 1988/03/03 | Expiration Date Change |
018024 | 023 | AP | 1984/11/28 | Formulation Revision |
018024 | 022 | AP | 1984/09/13 | Manufacturing Change or Addition |
018024 | 021 | AP | 1984/09/13 | Manufacturing Change or Addition |
018024 | 020 | AP | 1984/09/17 | Control Supplement |
018024 | 019 | AP | 1983/08/17 | Manufacturing Change or Addition |
018024 | 018 | AP | 1983/08/17 | Manufacturing Change or Addition |
018024 | 017 | AP | 1983/02/16 | Labeling Revision |
018024 | 016 | AP | 1986/10/23 | New or Modified Indication |
018024 | 015 | AP | 1984/03/02 | Expiration Date Change |
018024 | 014 | AP | 1984/03/02 | Formulation Revision |
018024 | 013 | AP | 1982/05/20 | Manufacturing Change or Addition |
018024 | 012 | AP | 1982/05/20 | Package Change |
018024 | 011 | AP | 1982/05/27 | Expiration Date Change |
018024 | 010 | AP | 1982/05/27 | Formulation Revision |
018024 | 007 | AP | 1981/04/01 | Manufacturing Change or Addition |
018024 | 006 | AP | 1981/02/20 | Manufacturing Change or Addition |
018024 | 003 | AP | 1980/02/21 | Manufacturing Change or Addition |
018024 | 002 | AP | 1980/01/24 | Manufacturing Change or Addition |
018024 | 001 | AP | 1979/06/28 | Labeling Revision |
018024 | 000 | AP | 1979/05/15 | Approval |