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) 071639
Active Ingredient(s):
IBUPROFEN
Company:
VINTAGE PHARMS
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071639
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/25/1991
007
Chemistry
5/3/1991
004
Chemistry
6/9/1988
002
Chemistry
6/9/1988
001
Chemistry
2/2/1988
000
Approval
Therapeutic Equivalents
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