Ordering Recommendation
Mnemonic
DULOX SP
Methodology

Quantitative High Performance Liquid Chromatography/Tandem Mass Spectrometry

Performed

Varies

Reported

7-10 days

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect

Plain Red, Lavender (K2EDTA), or Pink (K2EDTA).

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.4 mL) Requires light protection when submitted at Room Temperature.
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.

Storage/Transport Temperature

Refrigerated or frozen. Also acceptable: Room temperature (must be light protected).

Unacceptable Conditions

Separator tubes.

Remarks
Stability

Ambient: 1 month; Refrigerated: 1 month; Frozen: 1 year

Reference Interval

By Report

Interpretive Data



Compliance Category

Performed by non-ARUP Laboratory

Note
Hotline History
N/A
CPT Codes

80332 (Alt code: G0480)

Components
Component Test Code* Component Chart Name LOINC
2006474 Duloxetine Quantitative, Serum or Plasma 46227-5
* 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
  • Cymbalta(R)
Duloxetine Quantitative, Serum or Plasma

National Medical Services (NMS)