DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PRELONE
FDA Application No:
(ANDA) 089654
Active Ingredient(s):
PREDNISOLONE
Company:
MURO
Label History
Labels are not available on this site for PRELONE, (ANDA) 089654
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/9/2002
009
Facility Addition
7/28/1998
008
Labeling
4/1/1998
007
Labeling
6/23/1994
005
Labeling
7/2/1993
003
Labeling
7/2/1993
002
Chemistry
7/2/1993
001
Chemistry
1/17/1989
000
Approval
There are no Therapeutic Equivalents
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