What is the half-life of dicyclomine?

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Last updated: December 28, 2025View editorial policy

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Dicyclomine Half-Life

The elimination half-life of dicyclomine is approximately 1.8 hours based on initial plasma measurements, with a secondary elimination phase showing a somewhat longer half-life when measured up to 24 hours after dosing. 1

Pharmacokinetic Profile

The FDA-approved drug label provides the definitive pharmacokinetic data for dicyclomine:

  • Primary elimination half-life: approximately 1.8 hours when plasma concentrations were measured for 9 hours after a single oral dose 1
  • Secondary elimination phase: somewhat longer half-life detected in subsequent studies when plasma concentrations were followed for up to 24 hours, indicating biphasic elimination kinetics 1
  • Peak plasma concentrations: 60-90 minutes after oral administration 1
  • Volume of distribution: approximately 3.65 L/kg for a 20 mg oral dose, suggesting extensive tissue distribution 1

Elimination Pathways

Dicyclomine is primarily eliminated through renal excretion:

  • Urinary excretion: 79.5% of the administered dose 1
  • Fecal excretion: 8.4% of the dose 1
  • The metabolism of dicyclomine has not been systematically studied according to the FDA label 1

Clinical Implications

The relatively short half-life of dicyclomine has important dosing implications:

  • Multiple daily doses are required to maintain therapeutic effect, as the drug is rapidly eliminated from plasma 1
  • The biphasic elimination pattern (initial rapid phase followed by slower secondary phase) means that the clinically relevant terminal half-life is longer than the initial 1.8-hour measurement 1
  • Rapid absorption and elimination result in peak effects within 1-1.5 hours, with relatively short duration of action requiring frequent dosing intervals 1

Important Caveat

The presence of a secondary elimination phase with a longer half-life suggests that simple first-order kinetics may not fully describe dicyclomine's elimination, and accumulation with multiple dosing may differ from predictions based solely on the 1.8-hour half-life 1. This biphasic pattern is consistent with the drug's extensive tissue distribution (large volume of distribution of 3.65 L/kg) 1.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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