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) 074014
Active Ingredient(s):
KETOPROFEN
Company:
HERITAGE PHARMS INC
Label History
Labels are not available on this site for KETOPROFEN, (ANDA) 074014
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/7/1998
006
Chemistry
1/14/1998
005
Labeling
3/28/1995
004
Chemistry
3/28/1995
003
Chemistry
8/19/1994
002
Labeling
8/19/1994
001
Chemistry
1/29/1993
000
Approval
Therapeutic Equivalents
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