Ballicules › Drugs › Acamprosate
Pronunciation: a-KAM-pro-sayt
Mechanism of action: Acamprosate ballicule
Visual mnemonic: Acamprosate mascot“A camp roast” for alcohol use disorder standard dose is 666 mg T.I.D.
What it is Glutamatergic modulator — a negative modulator at the NMDA receptor polyamine site; maintenance of abstinence in alcohol use disorder.
Why this one It has no hepatic metabolism, so it is usable in liver disease where naltrexone is not.
What limits it Three-times-daily dosing with a large tablet burden. Renally cleared; it does not reduce craving in active drinking.
Molecular structure: Acamprosate
FDA-approved for
alcohol use disorder (2004)
FDA label
Read the full label on DailyMed ↗
FDA dosing Population Start Target Max
Maintenance of abstinence in alcohol dependence (abstinent at initiation) adult 666 mg TID 666 mg TID 666 mg TID
Renal Moderate (CrCl 30–50 mL/min): 333 mg TID; severe (CrCl ≤30 mL/min): contraindicated.
Hepatic Undefined
Instructions Initiate as soon as possible after alcohol withdrawal once abstinence is achieved; continue even if the patient relapses. Use as part of a comprehensive psychosocial treatment program. May be taken with or without food (dosing with meals may aid adherence). Swallow delayed-release tablets whole. Monitor for emergence of depression or suicidal ideation.
Available strengths
Contraindications Severe renal impairment (CrCl ≤30 mL/min)
Cautions Dose reduction required in moderate renal impairment Suicidality and depression — monitor patients and alert families/caregivers Does not eliminate or diminish alcohol withdrawal symptoms
Adverse reactions diarrhea, flatulence, nausea, anorexia, asthenia, pain, accidental injury, anxiety, depression, dizziness, dry mouth, insomnia, paresthesia, pruritus, sweating
Pregnancy Teratogenic in animals; use during pregnancy only if potential benefit justifies the potential fetal risk.
Lactation Unknown whether excreted in human milk (present in rat milk); exercise caution in nursing women.
Cost Acamprosate (CAMPRAL)
What pharmacies pay · NADAC 9/30/26
Strength #/mo generic $/mo CostPlus 333 mg DR tab 90 TID $53.02 offered
Generic entry 2013
Principal risk Three-times-daily dosing; renally cleared
Classes and tags
Clinical profile
Therapeutic safety burden 1 / 4
Overdose danger 1 / 4
Weight-gain liability 0 / 4
Sedation liability 0 / 4
QT / Torsades 0 / 4
Direct muscarinic antagonism 0 / 4
Embryofetal risk 1 / 4
Legacy pregnancy category Unknown / historical label unavailable
Defining liability Generally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.
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Memory aids: interaction avatars
no kinetic interactions
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