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) 071146
Active Ingredient(s):
IBUPROFEN
Company:
IVAX PHARMS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071146
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/5/1997
019
Chemistry
12/16/1992
018
Chemistry
12/16/1992
017
Chemistry
6/12/1991
016
Labeling
12/7/1990
015
Chemistry
12/7/1990
014
Chemistry
2/1/1989
013
Labeling
2/1/1989
012
Labeling
12/7/1990
011
Chemistry
1/11/1989
010
Chemistry
6/30/1988
008
Chemistry
6/30/1988
007
Chemistry
6/30/1988
006
Chemistry
4/6/1988
005
Chemistry
4/6/1988
004
Chemistry
8/26/1987
002
Chemistry
9/23/1986
000
Approval
Therapeutic Equivalents
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