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Drug analysis/clinical drug monitoring
For in vitro diagnostic use only
This test was developed, and its performance characteristics determined, by LabCorp. It has not been cleared or approved by the US Food and Drug Administration (FDA).
Plastic urine container
Urine temperature monitoring is recommended to ensure valid specimen collection.
Maintain specimen at room temperature. If arrival at lab will extend beyond seven days, refrigerate.
Causes for Rejection
Quantity not sufficient for analysis; incorrect specimen; incomplete specimen identification
This assay is intended for pain management. It is not intended for workplace testing and does not comply with state regulatory workplace testing programs.
|Order Code||Order Code Name||Order Loinc||Result Code||Result Code Name||UofM||Result LOINC|
|701900||Tapentadol, Urine||701902||Tapentadol, Urine||ng/mL||72485-6|
|701900||Tapentadol, Urine||733163||Please Note:||77202-0|