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) 070493
Active Ingredient(s):
IBUPROFEN
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070493
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
028
Chemistry
12/23/1994
026
Chemistry
10/11/1994
025
Chemistry
5/18/1993
024
Labeling
4/3/1992
023
Chemistry
4/3/1992
021
Chemistry
5/18/1993
020
Labeling
11/1/1991
018
Labeling Expedite
12/19/1988
014
Chemistry
8/2/1988
013
Chemistry
8/2/1988
011
Chemistry
5/7/1987
010
Chemistry
1/28/1987
009
Chemistry
1/28/1987
008
Chemistry
9/29/1986
006
Chemistry
9/29/1986
005
Chemistry
9/12/1986
003
Chemistry
7/10/1986
002
Chemistry
9/12/1986
001
Chemistry
12/24/1985
000
Approval
Therapeutic Equivalents
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