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) 071462
Active Ingredient(s):
IBUPROFEN
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071462
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
023
Chemistry
12/23/1994
022
Chemistry
10/11/1994
021
Chemistry
5/18/1993
020
Labeling
5/18/1993
019
Labeling
4/3/1992
018
Chemistry
4/3/1992
016
Chemistry
1/12/1995
015
Chemistry
1/12/1995
014
Chemistry
11/6/1991
013
Labeling Expedite
1/5/1989
009
Chemistry
7/6/1988
008
Chemistry
3/25/1987
005
Chemistry
8/27/1987
004
Chemistry
4/9/1987
003
Chemistry
4/9/1987
002
Chemistry
4/9/1987
001
Chemistry
10/2/1986
000
Approval
Therapeutic Equivalents
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