DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IBU
FDA Application No:
(ANDA) 070083
Active Ingredient(s):
IBUPROFEN
Company:
BASF
Label History
Labels are not available on this site for IBU, (ANDA) 070083
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/15/1995
020
Labeling
8/11/1995
019
Chemistry
9/30/1994
018
Chemistry
9/30/1994
017
Chemistry
5/3/1993
016
Labeling
3/11/1992
015
Labeling
10/24/1991
014
Labeling
8/6/1991
013
Labeling
9/6/1989
012
Labeling
2/14/1989
010
Labeling
2/14/1989
009
Chemistry
3/1/1988
008
Labeling
5/23/1986
006
Chemistry
1/16/1986
005
Chemistry
1/16/1986
004
Chemistry
1/16/1986
003
Chemistry
1/16/1986
002
Chemistry
2/22/1985
000
Approval
Therapeutic Equivalents
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