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) 071448
Active Ingredient(s):
IBUPROFEN
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071448
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/1/1998
016
Chemistry
12/23/1994
015
Chemistry
10/11/1994
014
Chemistry
4/3/1992
013
Chemistry
4/3/1992
011
Chemistry
8/12/1991
010
Labeling
9/20/1989
008
Labeling
7/12/1989
007
Labeling
12/16/1988
006
Chemistry
5/11/1988
004
Chemistry
5/11/1988
003
Chemistry
3/25/1987
001
Chemistry
2/18/1987
000
Approval
Therapeutic Equivalents
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