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Lidocaine 5% patch

Beijing Tiantan Hospital · FDA-approved active Small molecule

Lidocaine blocks sodium channels in nerve fibers, preventing the initiation and conduction of nerve impulses to produce local anesthesia.

Lidocaine blocks sodium channels in nerve fibers, preventing the initiation and conduction of nerve impulses to produce local anesthesia. Used for Postherpetic neuralgia (localized neuropathic pain), Localized pain relief.

At a glance

Generic nameLidocaine 5% patch
Also known asLidoderm, Lidoderm® (Endo Pharmaceuticals Inc, Malvern, PA, USA), Ebanel, UBER NUMB, Lidocaine patch
SponsorBeijing Tiantan Hospital
Drug classLocal anesthetic
TargetVoltage-gated sodium channels
ModalitySmall molecule
Therapeutic areaPain management / Dermatology
PhaseFDA-approved

Mechanism of action

Lidocaine is a local anesthetic that works by inhibiting sodium influx through sodium-selective channels in the nerve cell membrane, thereby preventing depolarization and blocking action potential propagation. When applied topically as a 5% patch, it penetrates the skin to anesthetize peripheral nerves in the area of application. This mechanism provides localized pain relief without systemic effects.

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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