| Action Date | Supplement Number | Approval Type | Letters, Reviews, Labels, Patient Package Insert |
|
10/1/2001
| 022 | Labeling Revision |
|
|
7/12/2001
| 021 | Control Supplement |
|
|
8/18/2000
| 019 | Labeling Revision |
|
|
2/21/1989
| 017 | Manufacturing Change or Addition |
|
|
6/28/1988
| 016 | Manufacturing Change or Addition |
|
|
6/28/1989
| 015 | Labeling Revision |
|
|
12/11/1987
| 014 | Control Supplement |
|
|
6/4/1987
| 013 | Control Supplement |
|
|
8/7/1985
| 012 | Control Supplement |
|
|
5/12/1987
| 011 | New or Modified Indication |
|
|
8/6/1985
| 010 | Control Supplement |
|
|
2/15/1986
| 009 | Labeling Revision |
|
|
5/12/1987
| 008 | Practioner Draft Labeling |
|
|
2/12/1982
| 007 | Control Supplement |
|
|
10/1/1981
| 006 | Labeling Revision |
|
|
5/30/1981
| 005 | Expiration Date Change |
|
|
1/14/1981
| 004 | Labeling Revision |
|
|
2/26/1982
| 003 | General Efficacy (MarkIV) |
|
|
6/16/1980
| 002 | Manufacturing Change or Addition |
|
|
2/7/1980
| 001 | Manufacturing Change or Addition |
|
|
9/19/1979
| 000 | Approval |
|