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

Nebivolol Hydrochloride Aurobindo

Active Ingredient:
Nebivolol
Origin:
EU

Nebivolol Hydrochloride Aurobindo (Nebivolol)

Nebivolol, the active ingredient in Nebivolol Hydrochloride Aurobindo, is a beta blocker presented as an oral tablet for oral use. It lowers elevated blood pressure and is prescribed for adults with primary hypertension. It is indicated for the management of high blood pressure and may be used as part of combination therapy when monotherapy is insufficient.

GNH India supplies Nebivolol Hydrochloride Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance, and reliable logistics for timely delivery.

Manufacturer / TM Owner

Aurobindo Pharma B.V.

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Indications & Clinical Uses

Nebivolol is a beta‑adrenergic blocker used primarily in the management of hypertension and related cardiovascular conditions.

  • Hypertension: reduces systolic and diastolic blood pressure in patients with primary hypertension.
  • Heart failure: improves cardiac output and may reduce hospitalization in patients with chronic heart failure with reduced ejection fraction.
  • Left ventricular hypertrophy: helps regress cardiac remodeling associated with high blood pressure.

How It Works

  • Nebivolol selectively antagonizes β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and contractility, which lowers cardiac output. In addition, it stimulates endothelial nitric oxide synthase, enhancing nitric oxide release and causing vasodilation of peripheral vessels. The combined β1‑blockade and nitric‑oxide‑mediated vasodilation result in a net reduction of systemic blood pressure. These actions also improve arterial compliance and reduce peripheral resistance, contributing further to antihypertensive effect.

Side Effects

Nebivolol may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate headache.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: general tiredness or reduced energy.
  • Nasal congestion: feeling of a blocked nose.
  • Peripheral edema: swelling of lower limbs.
  • Nausea: mild stomach upset.

Serious or Rare Side Effects

  • Bradycardia: abnormally slow heart rate that may require medical attention.
  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Bronchospasm: narrowing of airways, particularly in patients with asthma or COPD.
  • Allergic reaction: rash, itching, or swelling.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient-specific factors and monitor for potential complications.

  • Monitor blood pressure: regularly check to ensure therapeutic levels.
  • Assess heart rate: watch for bradycardia, especially in patients with conduction disorders.
  • Caution in hepatic impairment: dose adjustment may be needed in liver disease.
  • Avoid abrupt discontinuation: taper under medical supervision to prevent rebound hypertension.
  • Use with caution in asthma: β‑blockade may exacerbate bronchospasm.
  • Store at room temperature: keep below 25°C, retain original packaging, protect from moisture.

Avoid Interactions

Nebivolol can interact with several drug classes; careful review of a patient’s medication list is essential.

Major Interactions (Avoid)

  • Combined use with other β‑blockers: may cause excessive bradycardia and hypotension.
  • Concomitant calcium channel blockers (e.g., verapamil, diltiazem): increase nebivolol plasma levels.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): can raise drug concentration leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate antihypertensive effect, requiring blood pressure monitoring.
  • Antihyperglycemic agents: nebivolol may mask hypoglycemia symptoms.
  • NSAIDs: can reduce antihypertensive efficacy of nebivolol.

Frequently Asked Questions

Nebivolol Hydrochloride Aurobindo is prescribed to lower elevated blood pressure in adults with primary hypertension. It may also be used as part of combination therapy for patients with chronic heart failure or left ventricular hypertrophy when additional blood‑pressure control is needed.

Nebivolol selectively blocks β1‑adrenergic receptors in the heart, reducing heart rate and contractility. At the same time it stimulates endothelial nitric‑oxide synthase, increasing nitric‑oxide release and causing peripheral vasodilation. The dual effect lowers systemic vascular resistance and blood pressure.

The appropriate dose of Nebivolol is determined by the prescribing clinician based on the individual’s blood‑pressure profile, age, renal and hepatic function, and any concomitant therapies. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Nebivolol in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 is distinguished by its additional nitric‑oxide‑mediated vasodilatory activity, which may result in fewer metabolic side effects compared with non‑vasodilating beta‑blockers such as atenolol or metoprolol. Clinical choice depends on patient comorbidities, tolerance, and physician preference.

Nebivolol tablets should be stored at room temperature, below 25 °C, in the original container to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Nebivolol is taken orally, usually as a whole tablet swallowed with a glass of water. It is generally taken once daily, with or without food, as directed by the prescriber.

The most serious adverse events include marked bradycardia, severe hypotension, and bronchospasm, especially in patients with underlying cardiac conduction disorders or reactive airway disease. Prompt medical evaluation is required if any of these symptoms occur.

Nebivolol is contraindicated in patients with severe bradycardia, second‑ or third‑degree atrioventricular block, cardiogenic shock, or decompensated heart failure. Caution is also advised for individuals with uncontrolled asthma, severe hepatic impairment, or known hypersensitivity to the drug.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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