DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISOLONE
FDA Application No:
(ANDA) 085085
Active Ingredient(s):
PREDNISOLONE
Company:
WATSON LABS
Label History
Labels are not available on this site for PREDNISOLONE, (ANDA) 085085
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/6/1994
025
Labeling
1/6/1994
024
Labeling in Effect
3/3/1988
023
Labeling
12/1/1987
022
Chemistry
10/15/1987
020
Chemistry
10/15/1987
019
Chemistry
10/15/1987
018
Chemistry
10/15/1987
017
Chemistry
12/23/1986
016
Chemistry
2/14/1986
015
Chemistry
3/19/1984
014
Labeling
10/4/1982
009
Chemistry
3/29/1983
008
Chemistry
6/29/1976
000
Approval
Therapeutic Equivalents
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