DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FENOPROFEN CALCIUM
FDA Application No:
(ANDA) 072437
Active Ingredient(s):
FENOPROFEN CALCIUM
Company:
PAR PHARM
Label History
Labels are not available on this site for FENOPROFEN CALCIUM, (ANDA) 072437
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/31/1991
005
Labeling
5/12/1989
004
Labeling
3/31/1989
003
Labeling
8/22/1988
000
Approval
Therapeutic Equivalents
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