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Hydrocodone

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

Hydrocodone is a full opioid agonist primarily used for the management of moderate to severe pain requiring opioid-level analgesia. It acts on mu-opioid receptors in the central nervous system to produce its therapeutic effects. Due to its potential for dependence and abuse, it is classified as a Schedule II controlled substance.

Quick summary

Hydrocodone is an opioid analgesic used for moderate to severe pain that works by binding to mu-opioid receptors in the nervous system.

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

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
R05DA03
RxNorm
5489
Generic
Hydrocodone
Class
atc-r05
Brands
Ibudone, Zohydro, Hydromet, Verdrocet, Hysingla, Obredon, Hycofenix, Norco, Ventuss, Vicoprofen, Hy-KXP, Hycet, Tussionex, Reprexain, Hycodan
Availability
rx
Lactation
unknown
Routes
oral
Forms
suspension, 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
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: Single dose above 100mg may cause serious toxicity in opioid-naive individuals; lethal dose highly variable based on tolerance
Chronic overdose: prolonged use leading to physical dependence and respiratory depression
Immediate actions
ensure airway and breathing, administer naloxone, consider activated charcoal if within 1-2 hours of ingestion
Antidote
Naloxone(critical intervention, may require repeated dosing)
Poison Control: 1-800-222-1222

Special Populations

7 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks, particularly in first trimester

Monitor

regular fetal monitoring

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

avoid use near delivery due to risk of neonatal abstinence syndrome

Monitor

fetal monitoring and assessment for neonatal withdrawal symptoms

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

avoid breastfeeding during hydrocodone use due to infant exposure risk

Monitor

monitor infant for excessive sleepiness and respiratory depression

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

use lower initial doses and titrate slowly, monitor for sedation and falls

Monitor

regular assessment of pain control, sedation levels, and cognitive function

Use with caution and monitor for adverse effects.

✗

pediatric_age

children under 12
unsafe
FDA Category
C
Dose Adjustment

avoid

Key Recommendations

not recommended for use in children under 12 years of age

Monitor

if used, close monitoring of respiratory status required

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

⚠

renal_impairment

severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use reduced doses and extend dosing interval, monitor for accumulation

Monitor

monitor renal function and adjust dose accordingly

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
N
Dose Adjustment

reduce dose by 50%

Key Recommendations

use reduced doses due to impaired metabolism, avoid in severe impairment if possible

Monitor

monitor liver function and drug levels if available

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

Commonly prescribed since

Value:1990s

General prescribing information

drug_classWHO
2023

Drug class

Value:Opioid analgesic

Drug class information

usageMedical guidelines
2023

Common uses

Value:Pain management, cough suppression

Common therapeutic uses

regulatoryDEA
2023

Controlled substance schedule

Value:Schedule II (US)

Regulatory classification

Management of moderate to severe pain requiring opioid analgesia; also available in combination formulations with other medications such as acetaminophen or ibuprofen for enhanced pain relief.

Full opioid agonist with primary selectivity for mu-opioid receptors; produces analgesia by altering perception of pain and emotional response to pain in the central nervous system.

Carries significant risks of dependence, addiction, respiratory depression, and other opioid-related adverse effects; should be used with caution in patients with respiratory conditions, head injuries, or history of substance abuse; must be titrated carefully and discontinued gradually to avoid withdrawal symptoms.

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