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Articaine

Published: July 26, 2026Updated: July 26, 2026

Articaine is an amide-type local anesthetic used to induce temporary numbness in specific areas of the body during dental and minor surgical procedures. It works by blocking nerve signals in the targeted region, providing pain relief during procedures such as extractions, fillings, and other surgical interventions.

Quick summary

Articaine is a local anesthetic used to numb tissues during dental and minor surgical procedures.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
N01BB08
RxNorm
592464
Generic
Articaine
Class
atc-n01
Brands
Orabloc, Ultacan, Cyklx, Septocaine, Zorcaine, Articadent
Availability
rx
Pregnancy
C
Lactation
caution
Routes
ophthalmic
Forms
solution
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Consult local poison control center for specific information
Chronic overdose: Varies by patient
Immediate actions
Call poison control center: 1-800-222-1222
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid routine use during first trimester; use only if benefits clearly outweigh potential risks

Monitor

regular prenatal monitoring if use is necessary

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only when needed for dental procedures; avoid elective procedures

Monitor

standard prenatal care

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose, avoid high doses

Key Recommendations

use with caution; prolonged use or high doses may affect fetal heart rate

Monitor

fetal monitoring during prolonged procedures

Use with caution and monitor for adverse effects.

✓

lactation

breastfeeding
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

compatible with breastfeeding; no need to interrupt breastfeeding

Monitor

none required

✓

pediatric_age

children 2-12 years
safe
FDA Category
N
Dose Adjustment

dose based on weight, max 7mg/kg

Key Recommendations

use weight-based dosing; do not exceed maximum recommended dose

Monitor

standard pediatric monitoring

⚠

geriatric

over 65 years
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use lower doses due to increased sensitivity and reduced metabolism

Monitor

monitor for signs of toxicity and cardiovascular effects

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

no significant adjustment needed for mild-moderate

Key Recommendations

use standard doses with caution; monitor for accumulation

Monitor

monitor renal function periodically

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

consider dose reduction

Key Recommendations

use reduced doses and avoid repeated administrations

Monitor

close monitoring of renal function and for signs of toxicity

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

use with caution, no major dose reduction for mild

Key Recommendations

monitor for signs of accumulation; use lower doses for moderate

Monitor

monitor liver function and for toxicity signs

Use with caution and monitor for adverse effects.

✗

hepatic_impairment

severe
unsafe
FDA Category
N
Dose Adjustment

avoid or use minimal doses

Key Recommendations

avoid use in severe hepatic impairment due to impaired metabolism

Monitor

close monitoring if use is absolutely necessary

Use of this medication in this population requires careful consideration of risks and benefits.

Statistics and clinical data

drug_classFDA
2023

Drug class

Value:Amide local anesthetic

Articaine is classified as an amide-type local anesthetic

prescribingFDA
2023

FDA approval year

Value:2000

Year Articaine was approved for use in the United States

usageMedical guidelines
2023

Primary indication

Value:Local dental anesthesia

Primary clinical use for dental procedures

pharmacologyDrug information
2023

Onset of action

Value:2-3 minutes

Time to onset of anesthetic effect

Articaine is primarily used for local anesthesia in dental procedures including tooth extractions, fillings, root canal treatments, and oral surgeries. It may also be used for other minor surgical or diagnostic procedures requiring localized numbness and pain control.

As an amide local anesthetic, Articaine blocks the generation and conduction of nerve impulses by increasing the threshold for electrical excitation in nerve fibers, slowing the propagation of nerve impulses, and reducing the rate of depolarization, resulting in temporary localized numbness in the administered area.

Should only be administered by qualified healthcare professionals. Duration of action varies based on dosage and whether a vasoconstrictor is included. Contraindicated in patients with known hypersensitivity to amide anesthetics. May cause systemic effects if absorbed in large amounts or administered intravascularly. Pregnancy category C; use during pregnancy only if benefits outweigh risks.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy