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

Nebivolol Sandoz

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Sandoz (Nebivolol Hydrochloride)

Nebivolol Hydrochloride, the active ingredient in Nebivolol Sandoz, is a beta‑adrenergic blocker presented as an oral tablet for oral use. It is prescribed to manage hypertension and to improve outcomes in patients with chronic heart failure by reducing heart rate and peripheral vascular resistance.

GNH India supplies Nebivolol Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network ensures consistent quality and regulatory compliance across markets. We adhere to stringent quality standards to meet the needs of diverse healthcare systems.

Manufacturer / TM Owner

Sandoz Pharmaceuticals D.D.

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Indications & Clinical Uses

Nebivolol is a selective β1‑adrenergic blocker used in cardiovascular disease management.

  • Hypertension: lowers blood pressure by decreasing cardiac output and peripheral vascular resistance.
  • Heart failure: improves left ventricular systolic function and reduces the risk of hospitalization.
  • Isolated systolic hypertension in elderly patients: provides effective blood pressure control with a favorable heart‑rate profile.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility. Concurrently, it stimulates endothelial nitric oxide synthase, enhancing nitric oxide release, which causes vasodilation and reduces peripheral vascular resistance, contributing to its antihypertensive and heart‑failure benefits.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or general weakness.
  • Bradycardia: slower than normal heart rate.
  • Nasal congestion or mild upper‑respiratory irritation.
  • Nausea or mild gastrointestinal upset.

Serious or Rare Side Effects

  • Severe bradycardia or symptomatic heart block.
  • Marked hypotension leading to syncope.
  • Acute bronchospasm in patients with reactive airway disease.
  • Allergic reactions such as rash, pruritus, or angioedema.
  • Worsening heart failure symptoms.
  • Hepatic enzyme elevations or liver injury.

Precautions & Warnings

Use of Nebivolol requires careful clinical assessment and monitoring.

  • Blood pressure monitoring: ensure adequate control and avoid excessive hypotension.
  • Renal or hepatic impairment: dose adjustment may be necessary.
  • Asthma or chronic obstructive pulmonary disease: use with caution due to potential bronchospasm.
  • Abrupt discontinuation: taper gradually to prevent rebound hypertension.
  • Diabetes mellitus: monitor blood glucose as beta‑blockade may mask hypoglycaemia symptoms.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nebivolol may interact with several drug classes; clinical judgment is essential.

Major Interactions (Avoid)

  • Combined use with other beta‑blockers: risk of excessive bradycardia and hypotension.
  • Calcium channel blockers verapamil or diltiazem: can potentiate negative cardiac effects.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): increase nebivolol plasma concentrations.

Moderate Interactions (Monitor Closely):\n- Non‑steroidal anti‑inflammatory drugs (NSAIDs): may reduce antihypertensive efficacy.

  • Diuretics: additive blood‑pressure lowering effect; monitor electrolytes.
  • Other antihypertensives (ACE inhibitors, ARBs): may require dose titration.
  • Insulin or oral hypoglycemics: beta‑blockade can mask hypoglycaemia signs.
  • Certain antidepressants (e.g., sertraline): monitor for bradycardia.

Frequently Asked Questions

Nebivolol Sandoz is prescribed to treat essential hypertension and to manage chronic heart failure. It helps lower blood pressure and improves cardiac function by reducing heart rate and peripheral vascular resistance.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, decreasing heart rate and contractility. It also stimulates nitric oxide release from the endothelium, causing vasodilation and lowering peripheral resistance, which together lower blood pressure and support heart‑failure treatment.

The appropriate dose of Nebivolol Sandoz is determined by the prescribing clinician based on the patient’s medical condition, response to therapy, and any comorbidities. Dosage adjustments may be required for renal or hepatic impairment.

Safety of Nebivolol Sandoz in pregnancy and lactation has not been definitively 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 healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Nebivolol differs from many traditional beta‑blockers by also enhancing nitric oxide‑mediated vasodilation, which can result in better blood‑pressure control with fewer metabolic side effects. Its high β1 selectivity reduces the risk of bronchospasm compared with non‑selective agents.

Nebivolol Sandoz tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Do not store in extreme heat or humidity to maintain product stability.

Nebivolol 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 heart block, marked hypotension, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as angioedema. Patients should seek immediate medical attention if they experience these symptoms.

Nebivolol Sandoz is contraindicated in patients with known hypersensitivity to nebivolol or any component of the formulation, in those with severe bradycardia, second‑ or third‑degree heart block without a pacemaker, and in patients with uncompensated heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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