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Duragesic reference fentanyl TDS

University of Maryland, Baltimore · FDA-approved active Small molecule

Duragesic reference fentanyl TDS is a Synthetic opioid agonist Small molecule drug developed by University of Maryland, Baltimore. It is currently FDA-approved for Chronic pain in opioid-tolerant patients, Cancer pain, Severe chronic non-cancer pain. Also known as: Brand name fentanyl TDS.

Fentanyl is a synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation.

Fentanyl is a synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation. Used for Chronic pain in opioid-tolerant patients, Cancer pain, Severe chronic non-cancer pain.

At a glance

Generic nameDuragesic reference fentanyl TDS
Also known asBrand name fentanyl TDS
SponsorUniversity of Maryland, Baltimore
Drug classSynthetic opioid agonist
TargetMu-opioid receptor (μ-OR)
ModalitySmall molecule
Therapeutic areaPain Management
PhaseFDA-approved

Mechanism of action

Fentanyl activates mu-opioid receptors throughout the brain and spinal cord, inhibiting pain signal transmission and modulating pain perception. The transdermal delivery system (Duragesic patch) provides sustained-release fentanyl over 72 hours, maintaining steady-state plasma concentrations for chronic pain management. TDS (three times daily) dosing refers to the typical patch replacement schedule.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Duragesic reference fentanyl TDS

What is Duragesic reference fentanyl TDS?

Duragesic reference fentanyl TDS is a Synthetic opioid agonist drug developed by University of Maryland, Baltimore, indicated for Chronic pain in opioid-tolerant patients, Cancer pain, Severe chronic non-cancer pain.

How does Duragesic reference fentanyl TDS work?

Fentanyl is a synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation.

What is Duragesic reference fentanyl TDS used for?

Duragesic reference fentanyl TDS is indicated for Chronic pain in opioid-tolerant patients, Cancer pain, Severe chronic non-cancer pain.

Who makes Duragesic reference fentanyl TDS?

Duragesic reference fentanyl TDS is developed and marketed by University of Maryland, Baltimore (see full University of Maryland, Baltimore pipeline at /company/university-of-maryland-baltimore).

Is Duragesic reference fentanyl TDS also known as anything else?

Duragesic reference fentanyl TDS is also known as Brand name fentanyl TDS.

What drug class is Duragesic reference fentanyl TDS in?

Duragesic reference fentanyl TDS belongs to the Synthetic opioid agonist class. See all Synthetic opioid agonist drugs at /class/synthetic-opioid-agonist.

What development phase is Duragesic reference fentanyl TDS in?

Duragesic reference fentanyl TDS is FDA-approved (marketed).

What are the side effects of Duragesic reference fentanyl TDS?

Common side effects of Duragesic reference fentanyl TDS include Constipation, Nausea, Dizziness, Somnolence, Headache, Respiratory depression.

What does Duragesic reference fentanyl TDS target?

Duragesic reference fentanyl TDS targets Mu-opioid receptor (μ-OR) and is a Synthetic opioid agonist.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing