Product image of Nebivololo Sandoz (Nebivolol Hydrochloride) supplied by GNH India

Nebivololo Sandoz

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivololo Sandoz (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivololo Sandoz, is a beta blocker presented as an oral tablet for oral use. It is indicated for the treatment of hypertension and heart failure in adult patients. Nebivololo Sandoz is supplied as a prescription‑only product and is marketed in the European Union.

GNH India supplies Nebivolo Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sandoz S.P.A.

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Indications & Clinical Uses

  • Nebivolol acts on the cardiovascular system to lower blood pressure and improve cardiac output, making it useful in several related conditions.
  • Hypertension: Reduces systolic and diastolic blood pressure, helping to prevent stroke and myocardial infarction.
  • Heart failure: Improves left‑ventricular ejection fraction and reduces symptoms of congestion, supporting long‑term disease management.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility. In addition, it stimulates endothelial nitric oxide synthase, enhancing nitric oxide release and causing vasodilation. The combined effect lowers systemic vascular resistance and arterial pressure without significant β2‑mediated bronchoconstriction.

Side Effects

Nebivolol is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or reduced exercise tolerance.
  • Bradycardia: heart rate below normal range.
  • Nausea or mild gastrointestinal upset.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Marked hypotension leading to syncope.
  • Bronchospasm in patients with underlying airway disease.
  • Allergic reactions such as rash, angioedema, or anaphylaxis.
  • Worsening heart failure symptoms, including pulmonary edema.

Precautions & Warnings

  • Nebivolol should be used with clinical vigilance and appropriate monitoring.
  • Monitor blood pressure: ensure target values are achieved without excessive drop.
  • Assess heart rate: watch for bradycardia, especially in patients on other rate‑lowering agents.
  • Use caution in asthma or COPD: β1‑selectivity reduces risk but bronchospasm can still occur.
  • Review renal and hepatic function: dose adjustment may be needed in impairment.
  • Avoid abrupt discontinuation: tapering reduces risk of rebound hypertension.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol can interact with several drug classes, influencing its safety and efficacy.

Major Interactions (Avoid)

  • Other β‑blockers: additive negative chronotropic effects.
  • Non‑dihydropyridine calcium‑channel blockers (e.g., verapamil, diltiazem): may cause severe bradycardia or AV block.
  • Clonidine: concurrent use can lead to marked hypotension.
  • Anti‑arrhythmic agents (e.g., amiodarone): increased risk of conduction disturbances.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may blunt antihypertensive response.
  • Diuretics: can potentiate hypotensive effect, monitor electrolytes.
  • Antidiabetic drugs: enhanced hypoglycaemia risk, observe glucose levels.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): may raise nebivolol plasma concentrations.
  • ACE inhibitors or ARBs: monitor for additive blood‑pressure lowering.

Frequently Asked Questions

Nebivololo Sandoz contains nebivolol, a beta‑blocker prescribed to lower high blood pressure and to treat chronic heart failure. It helps control hypertension and improves cardiac function in patients with reduced ejection fraction.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility. It also stimulates nitric‑oxide release from the endothelium, causing vasodilation. The combined actions lower systemic vascular resistance and arterial pressure.

The specific dose of Nebivololo Sandoz is determined by the prescribing clinician based on the patient’s condition, age, renal function and concomitant therapies. Dosage may be started low and titrated to achieve target blood‑pressure or heart‑failure goals.

Nebivolol’s safety in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified health‑care professional.

Enquiries are submitted via the product page on gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Compared with non‑selective β‑blockers, nebivolol offers β1‑selectivity and additional nitric‑oxide‑mediated vasodilation, which may result in fewer metabolic side effects and better tolerability. It is often considered alongside ACE inhibitors, ARBs or calcium‑channel blockers depending on patient profile.

Nebivololo Sandoz tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Do not store in bathrooms or near heat sources.

Nebivololo Sandoz is taken orally, usually once daily with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious risks include severe bradycardia, symptomatic hypotension, heart block, bronchospasm in patients with obstructive airway disease, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience fainting, rapid weight gain, or difficulty breathing.

Nebivolol is contraindicated in patients with known hypersensitivity to nebivolol or any excipients, those with severe bradycardia, second‑ or third‑degree AV block without a pacemaker, and patients in cardiogenic shock. Caution is advised in asthma, COPD and severe hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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