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 |
019415 | 030 | AP | 2002/04/15 | Control Supplement |
019415 | 028 | AP | 2000/12/28 | Control Supplement |
019415 | 027 | AP | 2000/06/19 | Control Supplement |
019415 | 026 | AP | 2000/08/31 | Manufacturing Change or Addition |
019415 | 025 | AP | 2000/07/18 | Control Supplement |
019415 | 024 | AP | 2000/01/21 | Control Supplement |
019415 | 023 | AP | 1999/05/20 | Manufacturing Change or Addition |
019415 | 022 | AP | 1999/04/01 | Control Supplement |
019415 | 021 | AP | 1999/11/24 | Labeling Revision |
019415 | 018 | AP | 1998/04/15 | Manufacturing Change or Addition |
019415 | 017 | AP | 1998/02/18 | Control Supplement |
019415 | 016 | AP | 1996/08/22 | Manufacturing Change or Addition |
019415 | 015 | AP | 1996/01/22 | Manufacturing Change or Addition |
019415 | 014 | AP | 1995/07/12 | Labeling Revision |
019415 | 013 | AP | 1995/08/29 | New Dosage Regimen |
019415 | 012 | AP | 1993/12/06 | Control Supplement |
019415 | 011 | AP | 1994/01/24 | Labeling Revision |
019415 | 010 | AP | 1994/03/28 | Labeling Revision |
019415 | 009 | AP | 1996/08/23 | New Route of Administration |
019415 | 008 | AP | 1994/05/31 | Manufacturing Change or Addition |
019415 | 006 | AP | 1991/01/17 | Control Supplement |
019415 | 004 | AP | 1990/03/14 | Expiration Date Change |
019415 | 002 | AP | 1988/04/25 | Labeling Revision |
019415 | 001 | AP | 1988/03/01 | New or Modified Indication |
019415 | 000 | AP | 1986/09/18 | Approval |