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 |
017351 | 037 | AP | 2014/10/03 | Manufacturing Change or Addition |
017351 | 030 | AP | 2003/12/05 | Labeling Revision |
017351 | 028 | AP | 2002/11/20 | Package Change |
017351 | 027 | AP | 2002/07/08 | Labeling Revision |
017351 | 026 | AP | 1999/12/01 | Manufacturing Change or Addition |
017351 | 025 | AP | 1999/08/05 | Package Change |
017351 | 024 | AP | 1998/08/21 | Manufacturing Change or Addition |
017351 | 023 | AP | 1998/06/08 | Manufacturing Change or Addition |
017351 | 022 | AP | 1998/03/16 | Manufacturing Change or Addition |
017351 | 021 | AP | 1996/12/27 | Manufacturing Change or Addition |
017351 | 020 | AP | 1996/12/27 | Package Change |
017351 | 019 | AP | 1997/05/13 | Manufacturing Change or Addition |
017351 | 018 | AP | 1996/11/29 | Manufacturing Change or Addition |
017351 | 017 | AP | 1996/03/28 | Manufacturing Change or Addition |
017351 | 016 | AP | 1995/07/17 | Control Supplement |
017351 | 015 | AP | 1995/05/02 | Package Change |
017351 | 014 | AP | 1994/12/05 | Manufacturing Change or Addition |
017351 | 013 | AP | 1993/11/05 | Package Change |
017351 | 012 | AP | 1993/10/15 | Labeling Revision |
017351 | 011 | AP | 1986/04/24 | Package Change |
017351 | 010 | AP | 1984/11/20 | Expiration Date Change |
017351 | 007 | AP | 1983/04/26 | Control Supplement |
017351 | 006 | AP | 1982/12/30 | Manufacturing Change or Addition |
017351 | 005 | AP | 1982/09/16 | Package Change |
017351 | 004 | AP | 1985/06/06 | Control Supplement |
017351 | 003 | AP | 1982/02/10 | Control Supplement |
017351 | 002 | AP | 1982/02/10 | Control Supplement |
017351 | 000 | AP | 1982/02/12 | Approval |