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) 088832
Active Ingredient(s):
PREDNISONE
Company:
WEST WARD
Label History
Labels are not available on this site for PREDNISONE, (ANDA) 088832
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/9/2002
019
Control Supplement
10/1/1998
018
Chemistry
6/29/1998
017
Chemistry
11/13/2000
016
Chemistry
11/18/1997
015
Chemistry
10/3/1995
014
Chemistry
10/3/1995
013
Chemistry
11/14/1994
012
Labeling
2/9/1994
011
Labeling
4/14/1994
010
Chemistry
2/14/1992
009
Chemistry in Effect
11/6/1990
008
Labeling
2/13/1991
007
Chemistry
11/9/1994
005
Chemistry
11/9/1994
004
Chemistry
11/9/1994
003
Labeling
10/6/1987
001
Chemistry
12/4/1985
000
Approval
Therapeutic Equivalents
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