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Buprenorphine

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

Buprenorphine is an opioid medication primarily used for the treatment of opioid use disorder and management of moderate to severe pain. As a partial agonist at mu-opioid receptors with antagonist activity at kappa-opioid receptors, it provides therapeutic effects with a reduced risk of respiratory depression compared to full opioid agonists. It is typically administered as a sublingual tablet.

Quick summary

Buprenorphine is an opioid medication used for opioid use disorder treatment and pain management, functioning as a partial agonist with a ceiling effect on respiratory depression.

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

Key facts at a glance

ATC
N02AE01
RxNorm
1819
Generic
Buprenorphine
Class
atc-n02
Brands
Zubsolv, Bunavail, Simbadol, Belbuca, Sublocade, Buprenex, Zorbium, Brixadi, Suboxone, BuTrans
Availability
rx
Lactation
unknown
Routes
sublingual, topical
Forms
prefilled syringe, injection, 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)sublingual tablet
Usual dose
16-32mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)sublingual tablet
Usual dose
1-6mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)sublingual tablet
Usual dose
8-16mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Doses exceeding 40mg sublingually may result in serious toxicity including significant respiratory depression, especially when combined with other CNS depressants
Chronic overdose: cumulative toxicity may occur with repeated supratherapeutic dosing particularly in combination with other opioids or sedatives
Immediate actions
ensure airway patency, provide ventilatory support, consider naloxone administration, monitor vital signs
Antidote
Naloxone(partial effectiveness due to buprenorphine's high affinity; may require repeated or higher dosing)
Poison Control: 1-800-222-1222

Special Populations

10 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose if benefits outweigh risks

Key Recommendations

consider continuing if already on buprenorphine for OUD as discontinuation may pose greater risk; avoid initiating unless clearly needed

Monitor

regular prenatal monitoring, fetal growth assessment

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

maintain stable dose, avoid abrupt discontinuation

Key Recommendations

continue maintenance therapy to prevent withdrawal and relapse; neonatal abstinence syndrome may occur in newborn

Monitor

fetal monitoring, prepare for neonatal abstinence syndrome assessment

Use with caution and monitor for adverse effects.

✓

lactation

breastfeeding
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

buprenorphine is compatible with breastfeeding; low infant exposure through milk

Monitor

monitor infant for excessive sedation or respiratory depression

⚠

geriatric

elderly over 65
caution
FDA Category
C
Dose Adjustment

start at lower dose, consider dose reduction

Key Recommendations

use reduced initial doses and titrate slowly; increased sensitivity to sedative effects

Monitor

monitor for respiratory depression, sedation, cognitive impairment

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children 2 12 years
caution
FDA Category
C
Dose Adjustment

weight-based dosing required

Key Recommendations

use in pediatric patients for pain management with careful titration; not recommended for OUD treatment in children under 16

Monitor

close monitoring of respiratory status, sedation levels

Use with caution and monitor for adverse effects.

⚠

pediatric_age

adolescents 12 17 years
caution
FDA Category
C
Dose Adjustment

adult dosing with careful titration

Key Recommendations

may be used for OUD treatment in adolescents with careful monitoring

Monitor

monitor for misuse, respiratory depression

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe renal impairment
caution
FDA Category
C
Dose Adjustment

reduce dose and extend dosing interval

Key Recommendations

buprenorphine is hepatically metabolized but metabolites may accumulate in severe renal impairment; use reduced doses

Monitor

monitor for accumulation, adjust dose based on response

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate hepatic impairment
caution
FDA Category
C
Dose Adjustment

reduce dose by approximately 50%

Key Recommendations

buprenorphine undergoes hepatic metabolism; impaired liver function affects drug clearance

Monitor

monitor liver function, adjust dose based on clinical response

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe hepatic impairment
caution
FDA Category
C
Dose Adjustment

significant dose reduction required

Key Recommendations

use with extreme caution; consider alternative therapy

Monitor

frequent monitoring of liver function and drug response

Use with caution and monitor for adverse effects.

✗

alcohol_users

concurrent alcohol use
unsafe
FDA Category
C
Dose Adjustment

avoid concurrent use

Key Recommendations

alcohol increases risk of respiratory depression and sedation; avoid combining buprenorphine with alcohol

Monitor

monitor for respiratory depression, excessive sedation

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

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2002

FDA approval for opioid dependence treatment

drug_classWHO
2023

Drug class

Value:Partial opioid agonist

Pharmacological classification

usageSAMHSA
2023

Common uses

Value:Opioid use disorder treatment, pain management

Therapeutic applications

prescribingDEA
2023

Controlled substance schedule

Value:Schedule III

Regulatory classification

FDA-approved for the treatment of opioid use disorder (maintenance therapy) and management of moderate to severe pain. The sublingual formulation is primarily used for medication-assisted treatment of opioid dependence.

As a partial agonist at the mu-opioid receptor, buprenorphine activates the receptor to a lesser degree than full agonists, providing analgesic effects. Its antagonist activity at the kappa-opioid receptor may contribute to reduced dysphoria and anti-depressive effects.

Has a lower risk of respiratory depression than full opioid agonists due to its partial agonist properties. Can precipitate withdrawal in opioid-dependent patients if administered too soon after a full agonist. Common side effects include nausea, headache, and constipation. Has potential for dependence and should be used as part of a comprehensive treatment program.

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