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) 071769
Active Ingredient(s):
IBUPROFEN
Company:
IVAX PHARMS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071769
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/5/1997
014
Chemistry
12/16/1992
013
Chemistry
12/16/1992
012
Chemistry
8/22/1991
011
Labeling
12/7/1990
010
Chemistry
2/1/1989
009
Labeling
2/1/1989
008
Labeling
12/7/1990
007
Chemistry
1/13/1989
006
Chemistry
6/30/1988
005
Chemistry
6/30/1988
004
Chemistry
6/30/1988
003
Chemistry
8/30/1988
002
Chemistry
5/8/1987
000
Approval
Therapeutic Equivalents
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