DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KETOPROFEN
FDA Application No:
(ANDA) 073515
Active Ingredient(s):
KETOPROFEN
Company:
TEVA
Label History
Labels are not available on this site for KETOPROFEN, (ANDA) 073515
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/26/1999
012
Chemistry
7/14/1998
011
Chemistry
12/10/1997
010
Chemistry
5/13/1997
009
Chemistry
3/17/1998
008
Labeling
3/14/1997
007
Chemistry
3/14/1997
006
Chemistry
2/16/1995
003
Chemistry
9/6/1994
002
Chemistry
7/15/1994
001
Chemistry
12/22/1992
000
Approval
Therapeutic Equivalents
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