Last reviewed · How we verify

Lidocaine HCl 0.8% in D5W

Vanderbilt University Medical Center · FDA-approved active Small molecule

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

Lidocaine blocks sodium channels in nerve cell membranes, preventing the initiation and conduction of nerve impulses to produce local anesthesia. Used for Local and regional anesthesia, Ventricular arrhythmias (acute management).

At a glance

Generic nameLidocaine HCl 0.8% in D5W
SponsorVanderbilt University Medical Center
Drug classLocal anesthetic / Antiarrhythmic (Class IB)
TargetVoltage-gated sodium channels
ModalitySmall molecule
Therapeutic areaAnesthesia / Cardiology
PhaseFDA-approved

Mechanism of action

Lidocaine is a local anesthetic that works by inhibiting sodium influx through voltage-gated sodium channels in the neuronal cell membrane. This prevents depolarization and the generation of action potentials, thereby blocking pain signal transmission. The 0.8% concentration in D5W (dextrose 5% in water) is formulated for intravenous infusion, typically used for systemic anesthetic or antiarrhythmic effects.

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: