DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IBUPROFEN
FDA Application No:
(ANDA) 072096
Active Ingredient(s):
IBUPROFEN
Company:
PERRIGO
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 072096
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/26/2002
042
Control Supplement
11/26/2002
041
Control Supplement
11/26/2002
040
Control Supplement
9/12/2001
037
Labeling
8/21/2001
036
Control Supplement
8/21/2001
035
Package Change
10/26/2000
034
Labeling
6/19/2001
032
Facility Addition
3/27/2000
031
Control Supplement
10/1/1999
030
Control Supplement
3/11/1999
029
Labeling
6/23/1999
025
Chemistry
6/23/1999
024
Chemistry
7/15/1996
023
Labeling
7/25/1997
022
Chemistry
7/25/1997
021
Chemistry
3/22/1996
020
Chemistry
7/22/1996
019
Chemistry
6/1/1995
017
Chemistry
7/15/1996
016
Labeling
4/6/1995
015
Chemistry
2/13/1995
014
Chemistry
7/11/1994
013
Chemistry
7/6/1994
012
Chemistry in Effect
1/11/1994
011
Labeling
1/11/1994
010
Chemistry
11/15/1993
009
Chemistry
7/3/1991
008
Chemistry
11/30/1992
007
Chemistry
11/30/1992
006
Chemistry
2/11/1993
005
Chemistry
3/28/1989
001
Chemistry
12/8/1987
000
Approval
Therapeutic Equivalents
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