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) 085162
Active Ingredient(s):
PREDNISONE
Company:
WATSON LABS
Label History
Labels are not available on this site for PREDNISONE, (ANDA) 085162
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
048
Control Supplement
11/20/1998
044
Chemistry
6/12/1998
043
Chemistry
6/16/1997
042
Chemistry
11/14/1995
041
Labeling
2/8/1994
040
Labeling
1/28/1991
037
Chemistry
8/7/1991
036
Chemistry
6/29/1990
035
Chemistry
9/9/1988
034
Chemistry
9/9/1988
033
Chemistry
11/23/1987
032
Chemistry
11/23/1987
031
Chemistry
3/29/1984
027
Chemistry
1/16/1984
026
Chemistry
11/22/1983
025
Chemistry
9/7/1983
024
Chemistry
9/7/1983
022
Chemistry
11/12/1976
000
Approval
Therapeutic Equivalents
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