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) 072098
Active Ingredient(s):
IBUPROFEN
Company:
PERRIGO
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 072098
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/12/2001
032
Labeling
8/21/2001
031
Control Supplement
8/21/2001
030
Package Change
10/26/2000
029
Labeling
3/27/2000
027
Control Supplement
10/1/1999
026
Control Supplement
3/11/1999
025
Labeling
8/16/1999
023
Chemistry
7/25/1997
021
Labeling
7/25/1997
020
Chemistry
7/25/1997
019
Chemistry
3/22/1996
018
Chemistry
7/22/1996
017
Chemistry
6/1/1995
015
Chemistry
11/25/1996
014
Labeling
4/6/1995
013
Chemistry
2/13/1995
012
Chemistry
7/11/1994
011
Chemistry
7/6/1994
010
Chemistry
1/26/1994
009
Labeling
1/26/1994
008
Chemistry
11/30/1992
007
Chemistry
11/30/1992
006
Chemistry
2/11/1993
005
Chemistry
11/30/1992
004
Chemistry
3/28/1989
001
Chemistry
12/8/1987
000
Approval
Therapeutic Equivalents
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