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Exparel Injectable Solution

The Cooper Health System · FDA-approved active Small molecule

Liposomal bupivacaine is an encapsulated local anesthetic that blocks nerve impulses by inhibiting sodium channel activity, providing prolonged pain relief after surgical procedures.

Exparel (liposomal bupivacaine) is a marketed local anesthetic by Cooper Health System indicated for infiltration analgesia in patients 6+ years and regional nerve blocks in adults, generating $701M in revenue. The drug utilizes liposomal encapsulation technology to extend bupivacaine's duration of action, providing prolonged analgesia for up to 72 hours compared to conventional formulations. With 42 clinical trials and 4 publications supporting its efficacy, Exparel represents a significant advancement in perioperative pain management, reducing opioid requirements and improving patient outcomes across surgical specialties.

At a glance

Generic nameExparel Injectable Solution
SponsorThe Cooper Health System
Drug classLocal anesthetic (liposomal formulation)
TargetVoltage-gated sodium channels
ModalitySmall molecule
Therapeutic areaPain Management / Anesthesia
PhaseFDA-approved

Mechanism of action

Bupivacaine, a long-acting amide local anesthetic, works by blocking voltage-gated sodium channels in nerve cell membranes, which prevents the generation and conduction of action potentials. The liposomal formulation encapsulates the drug in lipid vesicles, allowing for sustained release and extended duration of anesthesia (up to 72 hours) compared to conventional bupivacaine. This enables single-dose infiltration at the surgical site for postoperative analgesia without repeated dosing.

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

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