Fentanyl Screen, Qualitative, Urine




Test Mnemonic

UFENTS

CPT Codes

  • 80307 - QTY (1)

LOINC ®

59673-4

Performing Laboratory

Cleveland Clinic Laboratories

FDA Category

In Vitro Diagnostic


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
3 mL Urine Yellow No additive Refrigerated 

Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
3 mL Urine Yellow No additive   

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
3 mL     

Stability

Environmental Condition Description
Ambient4 weeks
Refrigerated4 weeks
Frozen6 months

Days Performed

7 days a week

Turnaround Time

8 hours

Methodology

Name Description
Enzyme Immunoassay (EIA) 

Reference Range

Special Info

Preliminary positive results should be confirmed by another method.

Clinical Info

Evaluation of suspected acute overdose. This test should not be used for therapeutic drug or compliance monitoring; the quantitative pain panel, urine (UQNTPP) should be ordered instead.