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Pharmacology · Drugs Acting on Adrenergic Synapses

Nadolol

Nadololum

Nadolol (Nadololum) is a medicinal product that is a non-selective $\beta$-adrenergic blocker characterized by a prolonged therapeutic effect. Due to its pharmacological properties, the drug provides reliable control over cardiovascular pathologies with a single daily dose.

Pharmacological groupNon-selective $\beta$-adrenergic blocker
Half-lifeRanges from 20 to 24 hours
Dosing regimenOnce daily, regardless of food intake
ComparisonSimilar to propranolol, but with a longer duration of action
2 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Pharmacological profile

The drug nadolol belongs to the class of non-selective $\beta$-adrenergic blockers. This means that its action is not limited exclusively to cardiac receptors (unlike cardioselective drugs), but extends to $\beta$-adrenergic receptors in various locations.

In its basic pharmacological properties and receptor-binding profile, the drug is very close to the reference non-selective $\beta$-blocker, propranolol. However, the key difference of nadolol is a significantly greater duration of clinical effect, which determines the specifics of its prescription.

Pharmacokinetics and administration

The prolonged action of the drug is due to its pharmacokinetic parameters. The half-life ($t_{1/2}$) of nadolol is from 20 to 24 hours.

Such a prolonged elimination profile provides an important practical advantage:

  • The drug is prescribed in a dosing regimen of once daily.
  • Absorption efficiency and the drug's action do not depend on food intake, which significantly improves patient adherence to treatment.
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Indications for use

The spectrum of clinical application of nadolol covers both typical cardiological pathologies and endocrine disorders accompanied by hyperactivation of the sympathoadrenal system.

Key indications include:

  1. Arterial hypertension — for stable blood pressure reduction.
  2. Exertional angina — to reduce myocardial oxygen demand.
  3. Arrhythmias — to control and stabilize heart rhythm.
  4. Myocardial infarction — as part of combination therapy.
  5. Thyrotoxicosis — for relief of symptoms caused by excess thyroid hormones (tachycardia, tremor).

Briefly: answers to topical questions

How does nadolol differ from propranolol?

  • Nadolol differs from propranolol in its duration of effect, low lipophilicity, and lack of membrane-stabilizing activity.
PropertyNadololPropranolol
LipophilicityLow (hydrophilic)High (+++)
Duration of effectLong-acting—
Membrane-stabilizing activityAbsentPresent
How to memorize

You can remember the main difference between nadolol and its analog by the phonetic similarity: "NADOLOL is propranolol that works FOR A LONG TIME [RU: nadolgo] (24 hours)."

Class and exam questions

What group does nadolol belong to?

It is a long-acting non-selective $\beta$-adrenergic blocker.

What is the main difference between nadolol and propranolol?

Both drugs are non-selective $\beta$-blockers, but nadolol has a significantly longer duration of effect (half-life of 20–24 hours).

How does food intake affect nadolol dosing?

It has no effect. The drug is prescribed once daily regardless of food intake.

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What else to study on this topic

  • Mechanism of non-selective $\beta_1$- and $\beta_2$-adrenergic receptor blockade
  • Comparative profile of propranolol and nadolol
  • The role of $\beta$-adrenergic blockers in relieving symptoms of thyrotoxicosis
  • Pathogenesis of exertional angina and the sites of action of nadolol

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