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) 070436
Active Ingredient(s):
IBUPROFEN
Company:
WATSON LABS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070436
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/9/1991
020
Labeling
4/24/1991
019
Labeling
11/19/1990
017
Chemistry
8/7/1991
016
Chemistry
6/8/1989
014
SBA
6/29/1990
014
Chemistry
3/24/1989
013
Labeling
3/8/1989
012
SBA
6/15/1989
012
Chemistry
6/15/1989
011
Chemistry
4/15/1989
010
Chemistry
7/8/1988
009
Labeling
4/4/1988
008
Labeling
9/23/1992
007
Chemistry
10/28/1986
004
Chemistry
4/30/1986
002
Chemistry
3/25/1986
001
Chemistry
8/21/1985
000
Approval
Therapeutic Equivalents
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