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 |
017548 | 028 | AP | 1993/08/13 | Control Supplement |
017548 | 027 | AP | 1992/12/11 | Manufacturing Change or Addition |
017548 | 026 | AP | 1991/12/02 | Labeling Revision |
017548 | 025 | AP | 1990/10/18 | Control Supplement |
017548 | 023 | AP | 1990/10/18 | Control Supplement |
017548 | 022 | AP | 1990/08/24 | Manufacturing Change or Addition |
017548 | 021 | AP | 1989/11/09 | Control Supplement |
017548 | 020 | AP | 1988/01/11 | Manufacturing Change or Addition |
017548 | 018 | AP | 1983/02/04 | Control Supplement |
017548 | 016 | AP | 1982/03/24 | Manufacturing Change or Addition |
017548 | 015 | AP | 1981/10/09 | Manufacturing Change or Addition |
017548 | 014 | AP | 1987/04/08 | Practioner Draft Labeling |
017548 | 013 | AP | 1981/04/09 | Manufacturing Change or Addition |
017548 | 012 | AP | 1980/11/19 | Manufacturing Change or Addition |
017548 | 011 | AP | 1981/02/17 | Final Printed Labeling - MarkIV |
017548 | 010 | AP | 1979/03/29 | Labeling Revision |
017548 | 009 | AP | 1979/03/14 | Labeling Revision |
017548 | 008 | AP | 1978/11/30 | Control Supplement |
017548 | 007 | AP | 1978/12/07 | Distributor |
017548 | 006 | AP | 1977/08/11 | Expiration Date Change |
017548 | 003 | AP | 1975/04/03 | Control Supplement |
017548 | 002 | AP | 1975/02/21 | Control Supplement |
017548 | 001 | AP | 1974/10/08 | Control Supplement |
017548 | 000 | AP | 1974/07/29 | Approval |