| Action Date | Supplement Number | Approval Type | Letters, Reviews, Labels, Patient Package Insert |
|
1/7/2003
| 035 | Manufacturing Change or Addition |
|
|
12/13/1999
| 033 | Manufacturing Change or Addition |
|
|
12/22/1997
| 032 | Manufacturing Change or Addition |
|
|
12/22/1992
| 031 | Labeling Revision |
|
|
7/31/1992
| 030 | Labeling Revision |
|
|
7/12/1995
| 029 | Control Supplement |
|
|
7/26/1996
| 026 | Control Supplement |
|
|
8/25/1993
| 025 | Labeling Revision |
|
|
2/9/1989
| 023 | Labeling Revision |
|
|
10/19/1988
| 022 | Labeling Revision |
|
|
1/8/1985
| 021 | Manufacturing Change or Addition |
|
|
7/29/1985
| 020 | Labeling Revision |
|
|
9/19/1984
| 019 | Manufacturing Change or Addition |
|
|
10/4/1984
| 018 | Labeling Revision |
|
|
6/26/1984
| 016 | General Efficacy (MarkIV) |
|
|
12/19/1983
| 015 | General Efficacy (MarkIV) |
|
|
1/12/1983
| 014 | Manufacturing Change or Addition |
|
|
4/6/1982
| 013 | Manufacturing Change or Addition |
|
|
6/2/1981
| 012 | Control Supplement |
|
|
1/21/1980
| 011 | Distributor |
|
|
10/18/1979
| 010 | Formulation Revision |
|
|
9/18/1979
| 009 | Control Supplement |
|
|
1/25/1980
| 008 | Distributor |
|
|
5/29/1979
| 007 | Control Supplement |
|
|
1/8/1979
| 006 | Control Supplement |
|
|
10/3/1979
| 005 | Control Supplement |
|
|
1/8/1979
| 004 | Distributor |
|
|
7/13/1979
| 003 | Control Supplement |
|
|
1/8/1979
| 002 | Control Supplement |
|
|
11/15/1978
| 001 | Control Supplement |
|
|
2/10/1978
| 000 | Approval |
Review
|