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) 071163
Active Ingredient(s):
IBUPROFEN
Company:
OHM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071163
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/16/2001
039
Control Supplement
8/31/2001
038
Supplier Addition
9/18/2000
037
Manufacturing Revision
7/8/1999
035
Labeling
11/18/1998
034
Labeling
10/6/1997
032
Labeling
8/5/1994
031
Chemistry
7/29/1993
030
Labeling
11/2/1992
029
Labeling
9/21/1992
028
Chemistry
9/21/1992
027
Chemistry
4/21/1993
026
Labeling
4/21/1993
025
Chemistry
4/2/1990
024
Chemistry
1/18/1990
023
SBA
2/26/1990
023
Chemistry
6/22/1989
021
Labeling
4/17/1990
020
Chemistry
5/18/1989
019
Chemistry
11/22/1988
018
Chemistry
11/22/1988
017
Chemistry
11/21/1991
016
Labeling
11/21/1991
015
Chemistry
11/21/1991
014
Chemistry
5/31/1989
013
Chemistry
5/31/1989
012
Labeling
6/3/1988
011
Chemistry
4/28/1988
010
Chemistry
4/28/1988
009
Chemistry
12/9/1986
005
Chemistry
2/10/1987
004
Chemistry
10/3/1986
002
Chemistry
10/3/1986
001
Chemistry
7/15/1986
000
Approval
Therapeutic Equivalents
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