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) 071575
Active Ingredient(s):
IBUPROFEN
Company:
PAR PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071575
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/8/2001
026
Labeling
6/8/2001
025
Package Change
11/5/1998
024
Chemistry
1/14/1997
022
Chemistry
7/12/1996
021
Chemistry
7/15/1994
018
Chemistry
5/13/1996
017
Chemistry in Effect
10/26/1988
016
SBA
3/3/1989
013
Chemistry
3/3/1989
012
Chemistry
3/3/1989
010
Chemistry
12/15/1987
009
Chemistry
12/15/1987
008
Chemistry
9/9/1987
006
Chemistry
9/9/1987
005
Chemistry
5/8/1987
000
Approval
Therapeutic Equivalents
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