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Memantine

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

Memantine is an NMDA receptor antagonist used to treat moderate to severe Alzheimer's disease. It works by reducing excessive glutamate activity at NMDA receptors in the brain, which may help improve cognitive function, memory, and daily living abilities in patients with dementia. This medication is typically used when cholinesterase inhibitors alone are not sufficiently effective.

Quick summary

Memantine is an Alzheimer's medication that blocks NMDA receptors to reduce harmful glutamate activity in the brain.

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

Key facts at a glance

ATC
N06DX01
RxNorm
6719
Generic
Memantine
Class
atc-n06
Brands
Namzaric, Namenda
Availability
rx
Lactation
unknown
Routes
oral
Forms
capsule, tablet, 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
10mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
5mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
10mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Doses above 400mg have been associated with serious toxicity including neurological and cardiovascular effects
Chronic overdose: No significant cumulative toxicity reported; however, prolonged supratherapeutic dosing may lead to CNS effects
Immediate actions
Supportive care, gastric lavage if within 1-2 hours of ingestion, activated charcoal may be considered, monitor vital signs and cardiac function
Antidote
No specific antidote exists; treatment is supportive and symptomatic(Supportive care is the mainstay of treatment; early intervention improves outcomes)
Poison Control: 1-800-222-1222

Special Populations

12 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits to mother outweigh potential risks to fetus

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

use only if benefits to mother outweigh potential risks to fetus

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

discontinue near term if possible, use only if benefits outweigh risks

Monitor

fetal monitoring and assessment at delivery

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

discontinue breastfeeding

Key Recommendations

memantine is excreted in breast milk, breastfeeding should be discontinued

Monitor

infant monitoring for sedation and feeding problems

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

✓

geriatric

elderly
safe
FDA Category
C
Dose Adjustment

start low, go slow

Key Recommendations

initiate at 5mg daily, titrate to 10mg twice daily; monitor for dizziness and falls

Monitor

regular assessment of renal function and adverse effects

✗

pediatric_age

children adolescents
unsafe
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

not approved for use in patients under 18 years of age

Monitor

not applicable

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

⚠

renal_impairment

mild renal impairment
caution
FDA Category
C
Dose Adjustment

no adjustment required

Key Recommendations

standard dosing may be used, monitor renal function periodically

Monitor

monitor creatinine clearance regularly

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate renal impairment
caution
FDA Category
C
Dose Adjustment

dose reduction required

Key Recommendations

reduce starting dose to 5mg daily, may increase to 5mg twice daily after one week

Monitor

monitor renal function and for adverse effects

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe renal impairment
caution
FDA Category
C
Dose Adjustment

significant dose reduction required

Key Recommendations

limit to 5mg twice daily maximum, consider further reduction based on tolerance

Monitor

close monitoring of renal function and adverse effects

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild hepatic impairment
safe
FDA Category
C
Dose Adjustment

no adjustment required

Key Recommendations

standard dosing recommended

Monitor

periodic liver function monitoring

⚠

hepatic_impairment

moderate hepatic impairment
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

start at 5mg daily, titrate slowly

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe hepatic impairment
caution
FDA Category
C
Dose Adjustment

use with extreme caution

Key Recommendations

limited data available, consider dose reduction

Monitor

close monitoring of liver function and clinical response

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2000

FDA approval for Alzheimer's disease treatment

drug_classWHO
2023

Drug class

Value:NMDA receptor antagonist

Pharmacological classification

usageFDA
2023

Primary indication

Value:Moderate to severe Alzheimer's disease

Therapeutic indication

pharmacologyFDA
2023

Mechanism of action

Value:NMDA receptor blockade

Pharmacodynamic properties

Memantine is FDA-approved for treating moderate to severe Alzheimer's disease. It may be used alone or in combination with cholinesterase inhibitors (such as donepezil or rivastigmine) for patients who have not responded adequately to monotherapy.

Memantine acts as a low-to-moderate affinity, uncompetitive NMDA receptor antagonist. It binds to the open channel of the receptor, reducing excessive calcium influx caused by high glutamate levels. This is thought to protect neurons from excitotoxic damage associated with Alzheimer's pathology.

Common side effects include dizziness, headache, confusion, and constipation. Memantine should be used with caution in patients with seizure disorders or severe renal impairment. It is not a cure for Alzheimer's but may help slow symptom progression. Dosage is typically started low and gradually increased to the target dose.

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