Economy 90ml 15 Panel Drug Test Cup with EtG, Fentanyl, Tramadol & ADLTX

Economy 15 Panel Screening with EtG, Fentanyl and Tramadol

This Economy 90ml 15 panel drug test cup with EtG, fentanyl and tramadol provides preliminary urine screening for 15 drug targets, including EtG/300, FEN/20 and TRA/100, plus pH, specific gravity and creatinine specimen-validity indicators.

Three separate specimen-validity indicators—pH, specific gravity and creatinine—are also included. These indicators are not additional drug panels and should be interpreted according to the supplied product instructions.

This configuration is intended for qualified forensic testing programs that need expanded screening coverage in a compact, single-use collection cup. It is labeled Forensic Use Only and is not a CLIA-waived or over-the-counter test.

Product Features

• Fifteen drug or drug-metabolite screening panels
• pH, specific gravity and creatinine indicators
• Leak-resistant screw-cap collection format
• Single-use and disposable
• Quantity pricing for high-volume orders

EtG, Fentanyl and Tramadol Screening in One Cup

This configuration is differentiated by three specialty screening targets:

• EtG/300: Screens for ethyl glucuronide, a metabolite associated with alcohol exposure. An EtG screen does not measure current impairment or determine precisely when alcohol was consumed.
• FEN/20: Provides a dedicated fentanyl screening panel. Fentanyl is not automatically detected by a standard opiate panel.
• TRA/100: Adds a separate tramadol screening panel. A general opiate panel should not be assumed to screen for tramadol.

Programs that need K2 and kratom instead of barbiturates and PCP can compare the Economy 15 panel cup with K2, kratom and tramadol.

What Does This 15 Panel Drug and Alcohol Test Detect?

This cup also includes separate pH, specific gravity and creatinine specimen-validity indicators. Always confirm the analytes, cutoffs and interpretation instructions against the current product packaging.

How to Use the 15 Panel Drug Test Cup

Always follow the instructions supplied with the exact product.

1. Inspect the sealed pouch, expiration date and storage conditions.
2. Collect the required urine specimen directly into the cup.
3. Secure the screw lid and place the cup upright on a flat surface.
4. Check the temperature indicator within the period stated in the instructions.
5. Expose or activate the testing area as directed.
6. Read the drug-panel and specimen-validity results at the specified interpretation time.
7. Do not interpret results after the permitted reading window.

How to Interpret the Results

• Control line and test line: Negative preliminary result.
• Control line without a test line: Preliminary non-negative result.
• Missing control line: Invalid result; repeat with a new device.
• Faint test line: Generally interpreted as negative when the control line is present, subject to the product instructions.

See our illustrated guide explaining how to read a drug test cup for additional educational information.

Specimen-Validity Indicators

The included pH, specific gravity and creatinine indicators provide additional information about the characteristics of the urine specimen.

Results outside the ranges established by the manufacturer may require additional review. These indicators can identify unusual specimen characteristics, but they do not independently prove that a donor intentionally altered the sample.

Follow the package insert for the correct interpretation ranges and any required follow-up procedure.

Forensic Use and Result Limitations

This product is labeled Forensic Use Only. It should be used only for the settings and purposes identified by the manufacturer, such as eligible law-enforcement, court, correctional or forensic laboratory programs.

This rapid cup provides preliminary qualitative screening results. It does not determine impairment, the quantity of a substance consumed or the exact time of use.

A presumptive non-negative result that could lead to a legal or other significant decision should be reviewed according to the organization’s written testing procedure and confirmed using an appropriate laboratory method.

For additional educational information, review our guides to drug test cutoff levels and general drug detection times.

Bulk and Wholesale Ordering

Quantity pricing is available directly on the product page. Qualifying orders of 100 or more cups receive free shipping, and eligible in-stock orders placed before 3:00 p.m. EST can ship the same business day.

For recurring purchasing, institutional procurement or higher-volume requirements, review our wholesale drug testing supplies or contact DrugTestingCup.com before ordering.

Frequently Asked Questions

Does this 15 panel drug test detect alcohol?

It includes an EtG panel with a listed cutoff of 300 ng/mL. EtG is an alcohol metabolite, but an EtG screen does not determine current impairment or establish the precise time alcohol was consumed.

Does this cup include fentanyl and tramadol?

Yes. The configuration includes a FEN panel at 20 ng/mL and a TRA panel at 100 ng/mL.

Are pH, specific gravity and creatinine part of the 15 panels?

No. They are separate specimen-validity indicators and are not counted among the 15 drug-screening panels.

Is this 15 panel drug test CLIA waived?

No. This specific product is labeled Forensic Use Only. Buyers requiring a clinical configuration should review the CLIA-waived 15 panel drug test cup.

How quickly can the results be read?

The listed result time is approximately five minutes. Follow the package insert because reading a result too early or after the permitted interpretation window can produce an incorrect interpretation.

What does a faint test line mean?

A faint test line is generally interpreted as negative when the control line is present. Always follow the interpretation instructions supplied with the exact device.

Does a non-negative screen prove that a drug was used?

No. The cup provides preliminary qualitative screening. Presumptive non-negative results should be reviewed under the applicable testing policy and confirmed by an appropriate laboratory method when required.