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) 071547
Active Ingredient(s):
IBUPROFEN
Company:
WATSON LABS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071547
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/9/1991
014
Labeling
8/9/1991
013
Labeling
11/19/1990
011
Chemistry
8/7/1991
010
Chemistry
7/10/1989
009
Labeling
6/8/1989
008
SBA
6/29/1990
008
Chemistry
9/23/1992
007
Chemistry
3/18/1992
006
Chemistry
2/16/1989
005
SBA
3/24/1989
005
Labeling
3/18/1992
004
Chemistry
3/18/1992
003
Chemistry
7/8/1988
002
Labeling
4/4/1988
001
Labeling
7/2/1987
000
Approval
Therapeutic Equivalents
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