| Action Date | Supplement Number | Approval Type | Letters, Reviews, Labels, Patient Package Insert |
|
1/16/2002
| 030 | Control Supplement |
|
|
2/2/2001
| 029 | Control Supplement |
|
|
9/1/2000
| 028 | Control Supplement |
|
|
1/20/2000
| 027 | Manufacturing Change or Addition |
|
|
12/9/1998
| 026 | Package Change |
|
|
8/11/1998
| 025 | Package Change |
|
|
4/26/1993
| 024 | New or Modified Indication |
|
|
4/15/1993
| 023 | Package Change |
|
|
10/8/1992
| 022 | Labeling Revision |
|
|
4/21/1993
| 021 | Package Change |
|
|
5/12/1992
| 020 | Labeling Revision |
|
|
4/14/1992
| 019 | Labeling Revision |
|
|
9/22/1993
| 018 | Manufacturing Change or Addition |
|
|
6/23/1992
| 017 | Control Supplement |
|
|
9/11/1990
| 014 | Control Supplement |
|
|
10/4/1988
| 013 | Control Supplement |
|
|
11/30/1990
| 012 | OTC Labeling |
|
|
6/18/1987
| 011 | Control Supplement |
|
|
9/12/1986
| 010 | Manufacturing Change or Addition |
|
|
5/20/1986
| 009 | Control Supplement |
|
|
7/24/1985
| 007 | Package Change |
|
|
8/17/1981
| 006 | Control Supplement |
|
|
10/9/1981
| 005 | Control Supplement |
|
|
12/4/1986
| 004 | Practioner Draft Labeling |
|
|
3/27/1981
| 003 | Control Supplement |
|
|
1/3/1980
| 002 | Package Change |
|
|
11/27/1979
| 001 | Distributor |
|
|
11/8/1978
| 000 | Approval |
|