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) 071144
Active Ingredient(s):
IBUPROFEN
Company:
IVAX PHARMS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071144
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/5/1997
020
Chemistry
1/8/1990
014
Chemistry
4/25/1989
013
Labeling
12/7/1990
012
Chemistry
1/11/1989
011
Chemistry
6/30/1988
009
Chemistry
6/30/1988
008
Chemistry
6/30/1988
007
Chemistry
4/6/1988
006
Chemistry
7/8/1988
005
Chemistry
7/8/1988
004
Labeling
12/16/1992
003
Chemistry
12/16/1992
002
Chemistry
12/16/1992
001
Labeling
1/20/1987
000
Approval
Therapeutic Equivalents
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