DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METHYLPREDNISOLONE
FDA Application No:
(ANDA) 088497
Active Ingredient(s):
METHYLPREDNISOLONE
Company:
DURAMED PHARMS BARR
Label History
Labels are not available on this site for METHYLPREDNISOLONE, (ANDA) 088497
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/19/2002
045
Facility Addition
9/16/2002
044
Labeling
9/16/2002
043
Labeling
7/22/2002
042
Package Change
7/22/2002
041
Packager Addition
8/16/2001
040
Control Supplement
2/12/1999
039
Chemistry
6/23/1997
038
Labeling
3/9/1995
037
Labeling
2/4/1994
036
Labeling in Effect
5/24/1993
035
Chemistry in Effect
11/16/1992
030
Chemistry
1/20/1995
025
Chemistry
7/12/1988
023
Labeling
3/11/1988
022
Labeling
2/12/1987
019
Chemistry
2/12/1987
018
Chemistry
2/12/1987
017
Chemistry
10/4/1988
015
Chemistry
10/4/1988
014
Chemistry
8/8/1986
013
Chemistry
8/8/1986
012
Chemistry
8/8/1986
011
Chemistry
7/17/1985
007
Chemistry
7/17/1985
006
Chemistry
7/17/1985
005
Chemistry
5/15/1986
004
Chemistry
10/1/1984
002
Chemistry
10/1/1984
001
Chemistry
2/21/1984
000
Approval
Therapeutic Equivalents
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