2025-00425. Mandatory Guidelines for Federal Workplace Drug Testing Programs-Authorized Testing Panels  

  • Report Nomenclature—Urine

    Urine
    Abbreviation Analyte
    Δ9THCC Δ-9-tetrahydrocannabinol-9-carboxylic acid.
    BZE Benzoylecgonine.
    COD Codeine.
    MOR Morphine.
    HYC Hydrocodone.
    HYM Hydromorphone.
    OXYC Oxycodone.
    OXYM Oxymorphone.
    6-AM 6-Acetylmorphine.
    PCP Phencyclidine.
    FENT Fentanyl.
    NFENT Norfentanyl.
    AMP Amphetamine.
    MAMP Methamphetamine.
    MDMA Methylenedioxymethamphetamine.
    MDA Methylenedioxyamphetamine.

    HHS Drug Testing Panel—Urine

    Initial test analyte Initial test cutoff 1 Confirmatory test analyte Confirmatory test cutoff
    Marijuana metabolite (Δ9THCC) 50 ng/mL. Δ9THCC 15 ng/mL.
    Cocaine metabolite (Benzoylecgonine) 150 ng/mL.2 Benzoylecgonine 100 ng/mL.
    Codeine/Morphine 2,000 ng/mL. Codeine Morphine 2,000 ng/mL. 4,000 ng/mL.
    Hydrocodone/Hydromorphone 300 ng/mL. Hydrocodone Hydromorphone 100 ng/mL. 100 ng/mL.
    Oxycodone/Oxymorphone 100 ng/mL. Oxycodone Oxymorphone 100 ng/mL. 100 ng/mL.
    6-Acetylmorphine 10 ng/mL. 6-Acetylmorphine 10 ng/mL.
    Phencyclidine 25 ng/mL. Phencyclidine 25 ng/mL.
    Fentanyl 3 1 ng/mL. Fentanyl Norfentanyl 1 ng/mL. 1 ng/mL.
    Amphetamine/Methamphetamine 500 ng/mL. Amphetamine Methamphetamine 250 ng/mL. 250 ng/mL.
    MDMA/MDA 500 ng/mL. Methylenedioxymethamphetamine Methylenedioxyamphetamine 250 ng/mL. 250 ng/mL.
    1For grouped analytes ( i.e., two or more analytes that are in the same drug class and have the same initial test cutoff):
    Immunoassay: The test must be calibrated with one analyte from the group identified as the target analyte. The cross-reactivity of the immunoassay to the other analyte(s) within the group must be 80 percent or greater; if not, separate immunoassays must be used for the analytes within the group. ( print page 4668)
    Alternate technology: Either one analyte or all analytes from the group must be used for calibration, depending on the technology. For a technology that measures a response from the entire group without differentiating between analytes ( e.g., an activity-based assay, a mass spectrometric assay that does not differentiate isobaric compounds), the laboratory must compare the result to the initial test cutoff. In the case of an alternate technology that differentiates and quantifies each analyte in the group, the laboratory must compare each analyte's result to the confirmatory test cutoff and reflex specimens with a positive initial test result to confirmatory testing.
    2Alternate technology (BZE): The confirmatory test cutoff must be used for an alternate technology initial test that is specific for the target analyte ( i.e., 100 ng/mL for benzoylecgonine).
    3  A fentanyl immunoassay must have at least 5% cross-reactivity to norfentanyl.

    HHS Biomarker Testing Panel—Urine

    SAMHSA has not yet authorized routine testing for any biomarker in urine. HHS-certified laboratories and instrumented initial test facilities (IITFs) may request authorization to test Federal agency specimens for a biomarker upon Medical Review Officer (MRO) request by submitting supporting documentation and assay validation records to the National Laboratory Certification Program (NLCP) for SAMHSA review and approval.

    Report Nomenclature—Oral Fluid

    Oral fluid
    Abbreviation Analyte
    Δ9THC Δ-9-tetrahydrocannabinol.
    COC Cocaine.
    BZE Benzoylecgonine.
    COD Codeine.
    MOR Morphine.
    HYC Hydrocodone.
    HYM Hydromorphone.
    OXYC Oxycodone.
    OXYM Oxymorphone.
    6-AM 6-Acetylmorphine.
    PCP Phencyclidine.
    FENT Fentanyl.
    AMP Amphetamine.
    MAMP Methamphetamine.
    MDMA Methylenedioxymethamphetamine.
    MDA Methylenedioxyamphetamine.

    HHS Drug Testing Panel—Oral Fluid

    HHS drug testing panel—undiluted (neat) oral fluid
    Initial test analyte Initial test cutoff 1 Confirmatory test analyte Confirmatory test cutoff
    Marijuana (Δ9THC) 4 ng/mL. Δ9THC 2 ng/mL.
    Cocaine/Benzoylecgonine 15 ng/mL. Cocaine Benzoylecgonine 8 ng/mL. 8 ng/mL.
    Codeine/Morphine 30 ng/mL. Codeine Morphine 15 ng/mL. 15 ng/mL.
    Hydrocodone/Hydromorphone 30 ng/mL. Hydrocodone Hydromorphone 15 ng/mL. 15 ng/mL.
    Oxycodone/Oxymorphone 30 ng/mL. Oxycodone Oxymorphone 15 ng/mL. 15 ng/mL.
    6-Acetylmorphine 4 ng/mL.2 6-Acetylmorphine 2 ng/mL.
    Phencyclidine 10 ng/mL. Phencyclidine 10 ng/mL.
    Fentanyl 4 ng/mL. Fentanyl 1 ng/mL.
    Amphetamine/Methamphetamine 50 ng/mL. Amphetamine Methamphetamine 25 ng/mL. 25 ng/mL.
    MDMA/MDA 50 ng/mL. Methylenedioxymethamphetamine Methylenedioxyamphetamine 25 ng/mL. 25 ng/mL.
    1For grouped analytes ( i.e., two or more analytes that are in the same drug class and have the same initial test cutoff):
    Immunoassay: The test must be calibrated with one analyte from the group identified as the target analyte. The cross reactivity of the immunoassay to the other analyte(s) within the group must be 80 percent or greater; if not, separate immunoassays must be used for the analytes within the group.
    Alternate technology: Either one analyte or all analytes from the group must be used for calibration, depending on the technology. For a technology that measures a response from the entire group without differentiating between analytes (e.g., an activity-based assay, a mass spectrometric assay that does not differentiate isobaric compounds), the laboratory must compare the result to the initial test cutoff. In the case of an alternate technology that differentiates and quantifies each analyte in the group, the laboratory must compare each analyte's result to the confirmatory test cutoff and reflex specimens with a positive initial test result to confirmatory testing.
    2Alternate technology (6-AM): The confirmatory test cutoff must be used for an alternate technology initial test that is specific for the target analyte ( i.e., 2 ng/mL for 6-AM).

Document Information

Effective Date:
7/7/2025
Published:
01/16/2025
Department:
Health and Human Services Department
Entry Type:
Rule
Action:
Issuance of authorized drug testing panels.
Document Number:
2025-00425
Dates:
The authorized drug testing panels and required report nomenclature are effective July 7, 2025.
Pages:
4662-4668 (7 pages)
PDF File:
2025-00425.pdf
CFR: (1)
42 CFR None