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) 087773
Active Ingredient(s):
PREDNISONE
Company:
WATSON LABS
Label History
Labels are not available on this site for PREDNISONE, (ANDA) 087773
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/3/1998
021
Chemistry
2/3/1998
020
Chemistry
2/3/1998
019
Chemistry
11/2/1994
018
Labeling
12/23/1993
017
Labeling in Effect
4/20/1989
016
SBA
2/5/1991
016
Labeling
9/30/1988
013
Chemistry
4/6/1988
012
Chemistry
4/6/1988
011
Chemistry
4/6/1988
010
Chemistry
9/5/1986
008
Chemistry
12/11/1986
007
Chemistry
7/13/1982
000
Approval
Therapeutic Equivalents
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