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) 072249
Active Ingredient(s):
IBUPROFEN
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 072249
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/5/1997
002
Chemistry
1/12/1994
001
Chemistry
1/10/1989
000
Approval
Therapeutic Equivalents
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