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Lidoderm 5 % Topical Patch

Oregon Health and Science University · FDA-approved active Small molecule

Lidocaine blocks sodium channels in nerve fibers, interrupting pain signal transmission when applied topically to the skin.

Lidocaine blocks sodium channels in nerve fibers, interrupting pain signal transmission when applied topically to the skin. Used for Postherpetic neuralgia (localized neuropathic pain), Localized pain relief.

At a glance

Generic nameLidoderm 5 % Topical Patch
Also known aslidocaine patch, Lidoderm
SponsorOregon Health and Science University
Drug classLocal anesthetic
TargetVoltage-gated sodium channels
ModalitySmall molecule
Therapeutic areaPain management / Dermatology
PhaseFDA-approved

Mechanism of action

Lidocaine is a local anesthetic that penetrates the skin and reversibly inhibits sodium influx in nerve membranes, preventing depolarization and conduction of pain impulses. The 5% patch formulation delivers lidocaine transdermally to provide localized analgesia without systemic absorption. This mechanism allows sustained pain relief in the area of application for up to 12 hours.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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