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) 071807
Active Ingredient(s):
IBUPROFEN
Company:
SANDOZ
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071807
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/29/1995
020
Chemistry
3/29/1995
019
Chemistry
12/15/1995
017
Chemistry
3/20/1996
016
Labeling
12/15/1995
015
Chemistry
12/15/1995
014
Chemistry
12/15/1995
013
Chemistry
2/9/1993
012
Chemistry
3/16/1992
010
Labeling
3/16/1992
009
Chemistry
3/16/1992
008
Labeling
3/16/1992
007
Chemistry
6/9/1989
005
Chemistry
6/9/1989
004
Chemistry
6/9/1989
003
Chemistry
8/31/1988
002
Chemistry
8/31/1988
001
Chemistry
2/25/1988
000
Approval
Therapeutic Equivalents
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