| Action Date | Supplement Number | Approval Type | Letters, Reviews, Labels, Patient Package Insert |
|
10/29/2003
| 023 | Labeling Revision |
Letter
|
|
12/13/2002
| 022 | Control Supplement |
|
|
6/21/2001
| 020 | Labeling Revision |
|
|
7/22/2002
| 019 | Labeling Revision |
Letter
|
|
4/17/2001
| 018 | Labeling Revision |
Letter
|
|
9/10/1999
| 017 | Manufacturing Change or Addition |
|
|
5/4/1998
| 016 | Control Supplement |
|
|
2/25/1998
| 015 | Labeling Revision |
|
|
7/3/1997
| 014 | Control Supplement |
|
|
7/2/1997
| 013 | Manufacturing Change or Addition |
|
|
7/1/1997
| 012 | Manufacturing Change or Addition |
|
|
7/3/1996
| 011 | Labeling Revision |
|
|
6/18/1996
| 010 | Manufacturing Change or Addition |
|
|
11/2/1995
| 009 | Control Supplement |
|
|
11/1/1995
| 008 | Control Supplement |
|
|
11/20/1995
| 007 | Manufacturing Change or Addition |
|
|
4/12/1996
| 006 | Labeling Revision |
|
|
5/26/1993
| 004 | Labeling Revision |
|
|
10/12/1994
| 003 | Labeling Revision |
|
|
5/7/1992
| 002 | Labeling Revision |
|
|
10/29/1993
| 001 | New or Modified Indication |
|
|
11/19/1991
| 000 | Approval |
Other Important Information from FDA
|