Purpose
Compliance or Abuse Monitoring
Method(s)
High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS)
Suggested CPT Code(s)
80368
New York State Approval Status

Approved

Turnaround Time

8 days

Test Includes
1 Eszopiclone / Zopiclone Imovane®; Lunesta® High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) ng/mL 2 Sleep Aid

Specimen Type
Urine
Requested Volume
1 mL
Minimum Volume
0.4 mL
Special Handling
None
Specimen Container
NMS Labs has no experimental or literature-based data regarding the choice of specific specimen collection containers for this test.

Additional Collection Instructions

Transport Temperature
Frozen
Light Protection
Not Required
Rejection Criteria
Received Room Temperature. Received Refrigerated.

Rejection criteria pertain to clinical specimen submissions only.

Stability
Room Temperature: Not Stable
Refrigerated: Not Stable
Frozen (-20 °C): 14 day(s)
1 Eszopiclone / Zopiclone Imovane®; Lunesta® High Performance Liquid Chromatography/ Tandem Mass Spectrometry (LC-MS/MS) ng/mL 2 Sleep Aid

Interface Map

LOINC® Information