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) 070437
Active Ingredient(s):
IBUPROFEN
Company:
WATSON LABS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070437
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/9/1991
019
Labeling
5/22/1991
018
Labeling
11/19/1990
016
Chemistry
8/7/1991
015
Chemistry
7/12/1989
014
Labeling
6/29/1990
013
Chemistry
3/24/1989
012
Labeling
3/8/1989
011
SBA
1/30/1992
011
Chemistry
1/30/1992
010
Chemistry
1/30/1992
009
Chemistry
7/8/1988
008
Labeling
6/8/1989
007
SBA
4/4/1988
007
Labeling
6/8/1989
006
SBA
9/23/1992
006
Chemistry
1/30/1987
005
Chemistry
10/28/1986
003
Chemistry
4/30/1986
002
Chemistry
3/29/1986
001
Chemistry
8/21/1985
000
Approval
Therapeutic Equivalents
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