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) 071999
Active Ingredient(s):
IBUPROFEN
Company:
MYLAN
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071999
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/25/1998
017
Chemistry
2/5/1998
016
Chemistry
5/5/1994
015
Chemistry in Effect
10/10/1991
012
Labeling
10/31/1991
011
Labeling Expedite
10/31/1991
010
Chemistry Expedite
4/24/1991
009
Labeling
1/31/1990
008
Chemistry
6/21/1988
004
Chemistry
6/21/1988
003
Chemistry
6/21/1988
002
Chemistry
4/4/1988
001
Labeling
12/3/1987
000
Approval
Therapeutic Equivalents
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