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) 070985
Active Ingredient(s):
IBUPROFEN
Company:
PAR PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 070985
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/8/2001
023
Labeling
6/8/2001
022
Package Change
12/9/1998
021
Chemistry
1/14/1997
019
Chemistry
8/28/1996
018
Labeling
8/28/1996
017
Chemistry
7/15/1994
013
Chemistry
5/13/1996
012
Chemistry in Effect
4/19/1994
011
Chemistry in Effect
10/26/1988
009
SBA
3/3/1989
009
Chemistry
3/3/1989
008
Chemistry
3/3/1989
007
Chemistry
2/4/1988
005
Chemistry
2/4/1988
002
Chemistry
10/2/1987
000
Approval
Therapeutic Equivalents
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