Ordering Recommendation

Preferred test to follow up presumptive results. For general screening, Propoxyphene, Urine Screen with Reflex to Quantitation (2012269) is preferred.

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Plain red, lavender (K2EDTA or K3EDTA), or pink (K2EDTA).

Specimen Preparation

Separate from cells within 2 hours. Transfer 2 mL serum or plasma to an ARUP standard transport tube. (Min: 0.7 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.

Storage/Transport Temperature

Frozen. Also acceptable: Room temperature and refrigerated.

Unacceptable Conditions

Polymer gel separation tube (SST or PST).

Remarks
Stability

Ambient: 2 weeks; Refrigerated: 2 weeks; Frozen: 3 months

Methodology

Quantitative Gas Chromatography-Mass Spectrometry (GC-MS)

Performed

Varies

Reported

8-11 days

Reference Interval

Refer to report

Interpretive Data



Compliance Category

Performed by non-ARUP Laboratory

Note

Amitriptyline is a known interference.

Hotline History

N/A

CPT Codes

80367

Components

Component Test Code* Component Chart Name LOINC
3003724 Propoxyphene, S/P 3543-6
3003725 Norpropoxyphene, S/P 10341-6
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Darvon
Propoxyphene and Metabolite, Serum or Plasma

National Medical Services (NMS)