| Action Date | Supplement Number | Approval Type | Letters, Reviews, Labels, Patient Package Insert |
|
11/8/1999
| 030 | Manufacturing Change or Addition |
|
|
6/16/1999
| 029 | Labeling Revision |
|
|
11/3/1998
| 028 | Labeling Revision |
|
|
9/23/1998
| 027 | Control Supplement |
|
|
2/2/1996
| 026 | Control Supplement |
|
|
8/30/1995
| 025 | Package Change |
|
|
2/17/1995
| 024 | Manufacturing Change or Addition |
|
|
4/25/1994
| 023 | Manufacturing Change or Addition |
|
|
4/25/1994
| 022 | Manufacturing Change or Addition |
|
|
4/1/1985
| 021 | Manufacturing Change or Addition |
|
|
5/3/1985
| 020 | Manufacturing Change or Addition |
|
|
11/19/1982
| 019 | Control Supplement |
|
|
9/10/1981
| 018 | Control Supplement |
|
|
9/10/1981
| 017 | Control Supplement |
|
|
3/23/1981
| 016 | Manufacturing Change or Addition |
|
|
2/25/1981
| 015 | Distributor |
|
|
9/25/1980
| 014 | Formulation Revision |
|
|
5/5/1981
| 013 | Distributor |
|
|
8/18/1980
| 010 | Expiration Date Change |
|
|
2/28/1980
| 009 | Distributor |
|
|
2/1/1980
| 005 | Distributor |
|
|
11/26/1979
| 004 | Labeling Revision |
|
|
10/26/1979
| 003 | Formulation Revision |
|
|
10/15/1979
| 002 | Control Supplement |
|
|
10/15/1979
| 001 | Control Supplement |
|
|
4/16/1979
| 000 | Approval |
|