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) 074024
Active Ingredient(s):
KETOPROFEN
Company:
SANDOZ
Label History
Labels are not available on this site for KETOPROFEN, (ANDA) 074024
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/22/1999
003
Chemistry
2/20/1998
002
Labeling
10/21/1996
001
Chemistry
12/29/1995
000
Approval
Therapeutic Equivalents
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