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) 070079
Active Ingredient(s):
IBUPROFEN
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070079
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
035
Chemistry
12/23/1994
034
Chemistry
10/11/1994
033
Chemistry
4/3/1992
032
Chemistry
4/3/1992
030
Chemistry
9/11/1991
029
Chemistry
9/11/1991
028
Chemistry
8/12/1991
027
Labeling
9/13/1989
026
Labeling
5/17/1989
025
Labeling
2/2/1989
024
Labeling
12/16/1988
023
Chemistry
9/20/1988
022
Labeling
3/4/1988
021
Chemistry
3/4/1988
018
Chemistry
3/27/1987
017
Chemistry
8/20/1991
012
Chemistry
12/6/1985
008
Chemistry
12/7/1985
006
Chemistry
12/6/1985
005
Chemistry
12/6/1985
004
Chemistry
9/16/1985
002
Chemistry
9/16/1985
001
Chemistry
7/24/1985
000
Approval
Therapeutic Equivalents
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