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) 071231
Active Ingredient(s):
IBUPROFEN
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071231
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/5/1997
016
Chemistry
2/24/1997
015
Chemistry
6/22/1995
014
Chemistry
1/12/1994
013
Chemistry
6/2/1992
012
Labeling
12/14/1992
011
Chemistry
11/29/1990
010
Chemistry
6/28/1989
009
Labeling
12/30/1988
007
Labeling
1/13/1989
006
Chemistry
10/11/1988
005
Labeling
1/13/1989
004
Chemistry
8/27/1987
003
Chemistry
8/27/1987
002
Chemistry
7/30/1987
001
Chemistry
10/22/1986
000
Approval
Therapeutic Equivalents
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