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 |
016030 | 043 | AP | 1995/10/25 | Control Supplement |
016030 | 042 | AP | 1994/04/21 | Control Supplement |
016030 | 041 | AP | 1991/10/23 | Manufacturing Change or Addition |
016030 | 040 | AP | 1990/09/17 | Manufacturing Change or Addition |
016030 | 039 | AP | 1987/09/23 | Manufacturing Change or Addition |
016030 | 038 | AP | 1987/09/23 | Manufacturing Change or Addition |
016030 | 037 | AP | 1986/06/20 | Labeling Revision |
016030 | 036 | AP | 1986/06/20 | Labeling Revision |
016030 | 035 | AP | 1986/06/20 | Labeling Revision |
016030 | 034 | AP | 1986/06/20 | Labeling Revision |
016030 | 033 | AP | 1985/02/04 | Package Change |
016030 | 032 | AP | 1984/03/16 | Package Change |
016030 | 031 | AP | 1983/10/25 | Package Change |
016030 | 030 | AP | 1983/09/09 | Package Change |
016030 | 029 | AP | 1983/04/14 | Labeling Revision |
016030 | 028 | AP | 1983/01/11 | Manufacturing Change or Addition |
016030 | 027 | AP | 1983/06/08 | Package Change |
016030 | 026 | AP | 1983/04/07 | Package Change |
016030 | 025 | AP | 1982/01/06 | Package Change |
016030 | 024 | AP | 1980/10/17 | Manufacturing Change or Addition |
016030 | 023 | AP | 1980/02/28 | Control Supplement |
016030 | 022 | AP | 1979/07/24 | Manufacturing Change or Addition |
016030 | 021 | AP | 1979/07/24 | Manufacturing Change or Addition |
016030 | 020 | AP | 1979/03/02 | Package Change |
016030 | 017 | AP | 1975/12/12 | Control Supplement |
016030 | 000 | AP | 1965/06/25 | Approval |