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

Nebivolol Ab

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Ab (Nebivolol Hydrochloride)

Nebivolol Hydrochloride, the active ingredient in Nebivolol Ab, is a beta‑adrenergic blocker presented as an oral tablet for oral administration. It selectively antagonizes β1‑adrenergic receptors while promoting nitric‑oxide‑mediated vasodilation, thereby lowering elevated blood pressure and supporting cardiac function in patients with chronic heart failure.

GNH India supplies Nebivolol Ab as a licensed, Good Distribution Practice‑compliant pharmaceutical product to hospitals, pharmacies and clinics across international markets, ensuring quality and regulatory conformity. Our supply chain adheres to EU pharmacopeial standards and includes temperature‑controlled logistics where required.

Manufacturer / TM Owner

Aurobindo N.V.

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Indications & Clinical Uses

Nebivolol is a selective β1‑blocker used in cardiovascular therapy, primarily to control blood pressure and improve heart function.

  • Hypertension: lowers systolic and diastolic blood pressure in patients with essential hypertension.
  • Heart failure: reduces mortality and hospitalisation in adults with chronic heart failure.
  • Reduced left ventricular ejection fraction: improves cardiac output in patients with decreased ejection fraction due to heart failure.

How It Works

  • Nebivolol Hydrochloride binds selectively to β1‑adrenergic receptors, blocking catecholamine‑induced stimulation of heart rate and contractility. In parallel, it enhances endothelial nitric‑oxide synthase activity, leading to nitric‑oxide‑mediated vasodilation. The combined effect reduces systemic vascular resistance and myocardial oxygen demand, resulting in lowered arterial pressure and improved cardiac efficiency in heart‑failure states.

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 upon standing.
  • Fatigue: feeling unusually tired or weak.
  • Nasal congestion: mild blockage of nasal passages.

Serious or Rare Side Effects

  • Bradycardia: abnormally slow heart rate requiring medical assessment.
  • Severe hypotension: marked drop in blood pressure that may cause fainting.
  • Bronchospasm: airway narrowing, particularly in patients with reactive airway disease.

Precautions & Warnings

Nebivolol should be used with caution in specific clinical situations.

  • Cardiovascular disease: assess baseline heart rate and blood pressure before initiation.
  • Renal impairment: dose adjustment may be needed in patients with reduced kidney function.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Concomitant β‑blockers: avoid additive effects that could cause excessive bradycardia.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Nebivolol may interact with several drug classes, requiring clinical vigilance.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., paroxetine, quinidine): can markedly increase nebivolol plasma levels.
  • Non‑selective β‑blockers: combined use may cause profound bradycardia and hypotension.
  • Severe bradyarrhythmias: concurrent use can exacerbate heart‑rate slowing.

Moderate Interactions (Monitor Closely):\n- Calcium‑channel blockers (e.g., amlodipine): may enhance antihypertensive effect.

  • Diuretics: additive blood‑pressure lowering, monitor electrolytes.
  • Other antihypertensives: dose titration may be required to avoid excessive hypotension.

Frequently Asked Questions

Nebivolol Ab is prescribed for adults with essential hypertension to lower blood pressure and for patients with chronic heart failure to improve cardiac function and reduce the risk of hospitalisation.

Nebivolol Hydrochloride selectively blocks β1‑adrenergic receptors, decreasing heart rate and contractility, while simultaneously stimulating nitric‑oxide release from the endothelium, which causes vasodilation and further reduces arterial pressure.

The appropriate dose of Nebivolol Ab is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any concomitant medications. Patients should follow the prescriber’s instructions exactly.

Safety data for Nebivolol in pregnancy and lactation are limited, and the product is classified as pregnancy category unknown. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and under close medical supervision.

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 is a highly selective β1‑blocker that also promotes nitric‑oxide‑mediated vasodilation, offering a dual mechanism not seen with many non‑selective beta‑blockers. This may result in better blood‑pressure control with fewer metabolic side effects, though individual response varies.

Nebivolol Ab should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children.

Nebivolol Ab is taken orally, usually once daily, with or without food, as directed by the prescribing healthcare professional. Swallow the tablet whole with a glass of water.

Serious risks include marked bradycardia, severe hypotension, and bronchospasm, especially in patients with pre‑existing cardiac conduction disorders or reactive airway disease. Prompt medical attention is required if these symptoms occur.

Nebivolol Ab is contraindicated in patients with known hypersensitivity to nebivolol or any excipients, in those with severe bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and in individuals with uncompensated heart failure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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