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

Nebivolol Zydus

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Zydus (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Zydus, is a beta blocker presented as an oral tablet for oral administration. It selectively antagonizes β1‑adrenergic receptors while stimulating nitric oxide release, resulting in vasodilation and reduced systemic vascular resistance, thereby lowering blood pressure in adult patients diagnosed with hypertension.

GNH India supplies Nebivolol Zydus as a licensed, GDP‑compliant international pharmaceutical product, providing reliable access to hospitals, pharmacies and clinics worldwide, and supporting therapeutic needs across the European Union market through established distribution networks and quality assurance processes.

Manufacturer / TM Owner

Zydus France

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Indications & Clinical Uses

Nebivolol Zydus is a beta‑blocker that acts on the cardiovascular system to control elevated blood pressure.

  • Essential hypertension: lowers systolic and diastolic blood pressure in adult patients.
  • Secondary hypertension: contributes to blood pressure control when hypertension is due to identifiable causes.
  • Isolated systolic hypertension: reduces elevated systolic pressure in older adults.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors on cardiac tissue, decreasing heart rate and contractility, while simultaneously enhancing endothelial nitric oxide synthase activity, which increases nitric oxide production and promotes vasodilation, together leading to reduced systemic vascular resistance and lower arterial pressure.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain in the head region.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Fatigue: unusual tiredness or lack of energy.
  • Bradycardia: slower than normal heart rate.
  • Nausea: feeling of stomach upset.
  • Peripheral edema: swelling of the lower limbs.

Serious or Rare Side Effects

  • Severe bradycardia: markedly slow heart rate requiring medical attention.
  • Hypotension: dangerously low blood pressure.
  • Atrioventricular block: impaired electrical conduction in the heart.
  • Bronchospasm: narrowing of airways, especially in asthmatic patients.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Liver enzyme elevation: abnormal liver function tests.

Precautions & Warnings

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

  • Blood pressure monitoring: check regularly to ensure therapeutic response.
  • Heart rate assessment: observe for bradycardia, especially in patients with pre‑existing slow heart rates.
  • Asthma or COPD caution: beta‑blockade may exacerbate bronchospasm.
  • Concomitant medications: review for drugs that also lower heart rate or blood pressure.
  • Renal impairment: consider dose adjustment in patients with reduced kidney function.
  • Store at ambient temperature: keep below 25°C in the original packaging, protect from moisture.

Avoid Interactions

Nebivolol can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Verapamil or diltiazem: combined use may cause profound bradycardia or AV block.
  • Other beta‑blockers: additive effects on heart rate and blood pressure.
  • CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): may increase nebivolol plasma concentrations.

Moderate Interactions (Monitor Closely):\n- Diuretics: may enhance hypotensive effect, requiring blood pressure monitoring.

  • Antihypertensive agents (ACE inhibitors, ARBs): may produce additive blood pressure lowering.
  • Antidiabetic drugs: nebivolol can mask hypoglycemia symptoms; monitor glucose levels.

Frequently Asked Questions

Nebivolol Zydus is prescribed to lower elevated blood pressure in adult patients with hypertension. By reducing systemic vascular resistance, it helps achieve target blood pressure levels and decreases the risk of cardiovascular complications associated with uncontrolled hypertension.

Nebivolol selectively blocks β1‑adrenergic receptors, decreasing heart rate and myocardial contractility. At the same time, it stimulates nitric oxide release from the endothelium, causing vasodilation. The combined effect lowers systemic vascular resistance and reduces arterial pressure.

The dose of Nebivolol Zydus is individualized by the prescribing clinician based on the patient’s blood pressure, age, renal function, and concomitant therapies. The prescriber determines the appropriate starting dose and any subsequent titration.

Safety data for Nebivolol in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It is generally avoided unless the potential benefit justifies the potential risk to the fetus or infant.

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 β1‑selective blocker that also enhances nitric oxide‑mediated vasodilation, which may result in fewer metabolic side effects compared with non‑selective agents like propranolol. Compared with metoprolol, nebivolol often provides similar blood‑pressure control with a lower incidence of fatigue and may improve endothelial function.

Nebivolol Zydus tablets should be stored at ambient temperature, preferably 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 after the expiry date.

Nebivolol Zydus is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare professional.

The most serious adverse events include severe bradycardia, marked hypotension, atrioventricular block, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as anaphylaxis. Prompt medical attention is required if any of these symptoms occur.

Nebivolol Zydus is contraindicated in patients with severe bradycardia (heart rate < 45 bpm), second‑ or third‑degree atrioventricular block, cardiogenic shock, or overt heart failure with low output. Caution is also advised for individuals with uncontrolled asthma or severe chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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