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) 070099
Active Ingredient(s):
IBUPROFEN
Company:
BASF
Label History
Labels are not available on this site for IBU, (ANDA) 070099
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/15/1995
027
Labeling
8/11/1995
026
Chemistry in Effect
3/20/1992
024
Labeling
10/17/1991
023
Labeling
8/3/1992
022
Chemistry
8/3/1992
021
Chemistry
8/6/1991
020
Labeling
8/16/1990
019
Chemistry in Effect
10/27/1989
018
Labeling
1/10/1989
016
Labeling
10/7/1988
015
Labeling
2/8/1988
014
Labeling
8/27/1987
010
Chemistry
8/27/1987
009
Chemistry
5/20/1986
007
Chemistry
5/20/1986
006
Chemistry
1/17/1986
005
Chemistry
10/7/1988
005
Labeling
1/17/1986
004
Chemistry
1/17/1986
003
Chemistry
1/17/1986
002
Chemistry
3/29/1985
000
Approval
Therapeutic Equivalents
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