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 |
010417 | 032 | AP | 2013/03/28 | Manufacturing Change or Addition |
010417 | 031 | AP | 2013/03/28 | Labeling Revision |
010417 | 027 | AP | 2010/02/19 | Labeling Revision |
010417 | 022 | AP | 1999/03/12 | Labeling Revision |
010417 | 021 | AP | 1996/03/11 | Manufacturing Change or Addition |
010417 | 020 | AP | 1995/07/11 | Control Supplement |
010417 | 019 | AP | 1996/09/13 | Expiration Date Change |
010417 | 018 | AP | 1994/11/22 | Manufacturing Change or Addition |
010417 | 017 | AP | 1993/02/18 | Manufacturing Change or Addition |
010417 | 016 | AP | 1989/07/11 | Control Supplement |
010417 | 015 | AP | 1987/09/16 | Manufacturing Change or Addition |
010417 | 014 | AP | 1984/06/20 | Manufacturing Change or Addition |
010417 | 013 | AP | 1982/06/28 | Manufacturing Change or Addition |
010417 | 012 | AP | 1982/03/25 | Control Supplement |
010417 | 011 | AP | 1985/03/25 | Practioner Draft Labeling |
010417 | 010 | AP | 1982/08/09 | Labeling Revision |
010417 | 009 | AP | 1982/08/09 | Control Supplement |
010417 | 008 | AP | 1980/11/03 | Labeling Revision |
010417 | 007 | AP | 1980/12/04 | Labeling Revision |
010417 | 006 | AP | 1980/12/04 | Package Change |
010417 | 005 | AP | 1980/11/03 | Control Supplement |
010417 | 004 | AP | 1979/08/29 | Labeling Revision |
010417 | 003 | AP | 1980/06/13 | Labeling Revision |
010417 | 002 | AP | 1973/02/01 | Labeling Revision |
010417 | 000 | AP | 1959/05/07 | Approval |