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) 070986
Active Ingredient(s):
IBUPROFEN
Company:
PAR PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070986
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/13/1998
032
Chemistry
1/14/1997
030
Chemistry
7/15/1994
027
Chemistry
4/8/1994
026
Chemistry in Effect
1/10/1992
025
Labeling
6/11/1991
024
Labeling
2/21/1989
022
Labeling
12/30/1988
021
Chemistry
12/30/1988
021
Labeling
11/22/1988
020
Chemistry
3/2/1989
019
Chemistry
3/2/1989
018
Chemistry
11/10/1988
017
SBA
3/2/1989
017
Chemistry
7/1/1988
016
Labeling
2/10/1988
012
Chemistry
9/22/1987
010
Chemistry
2/2/1988
009
Chemistry
7/20/1988
006
Chemistry
7/23/1987
005
Chemistry
10/17/1986
003
Chemistry
7/25/1986
000
Approval
Therapeutic Equivalents
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