DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MOTRIN
FDA Application No:
(NDA) 020418
Active Ingredient(s):
IBUPROFEN
Company:
MCNEIL PED
Label History
Labels are not available on this site for MOTRIN, (NDA) 020418
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/14/2001
004
Control Supplement
2/4/2002
003
Labeling Revision
Letter
Review
3/24/1995
001
New or Modified Indication
11/16/1994
000
Approval
Therapeutic Equivalents
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