DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISONE
FDA Application No:
(ANDA) 080356
Active Ingredient(s):
PREDNISONE
Company:
WATSON LABS
Label History
Labels are not available on this site for PREDNISONE, (ANDA) 080356
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
079
Control Supplement
6/15/1998
075
Chemistry
6/15/1998
074
Chemistry
6/16/1997
073
Chemistry
11/14/1995
072
Labeling
2/8/1994
071
Labeling
1/28/1991
068
Chemistry
6/29/1990
066
Chemistry
2/17/1988
065
Chemistry
2/17/1988
064
Chemistry
10/9/1987
063
Chemistry
9/8/1987
062
Chemistry
11/19/1987
061
Chemistry
11/19/1987
060
Chemistry
6/3/1985
058
Chemistry
6/3/1985
057
Chemistry
12/15/1983
055
Chemistry
12/8/1983
054
Chemistry
8/23/1983
053
Chemistry
7/20/1983
052
Chemistry
7/20/1983
051
Chemistry
3/30/1972
001
Chemistry
1/17/1972
000
Approval
Therapeutic Equivalents
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