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) 075010
Active Ingredient(s):
IBUPROFEN
Company:
LNK
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 075010
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/4/2005
007
Supplement
7/19/2004
006
Supplement
2/4/2003
005
Supplement
8/5/2003
004
Supplement
8/15/2002
003
Labeling
Review
9/27/2001
002
Manufacturing Revision
Review
11/20/2000
001
Formulation Revision
Review
3/1/1999
000
Approval
Letter
Review
Therapeutic Equivalents
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