DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FENTANYL
FDA Application No:
(NDA) 020195
Active Ingredient(s):
FENTANYL CITRATE
Company:
CEPHALON
Label History
Labels are not available on this site for FENTANYL, (NDA) 020195
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/1/2000
005
Formulation Revision
8/25/2000
004
Control Supplement
5/20/1996
002
Patient Population Altered
Review
10/30/1995
001
New Dosage Regimen
10/4/1993
000
Approval
There are no Therapeutic Equivalents
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