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

Nebicard

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebicard (Nebivolol Hydrochloride)

Nebivolol hydrochloride, the active ingredient in Nebicard, is a beta‑blocker presented as an oral tablet for oral use. It is employed to lower high blood pressure and to improve outcomes in patients with chronic heart failure, acting selectively on β1‑adrenergic receptors while enhancing nitric‑oxide mediated vasodilation.

GNH India supplies Nebicard as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to meet global demand through reliable logistics.

Manufacturer / TM Owner

Sandoz Pharmaceuticals D.D.

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Indications & Clinical Uses

  • Nebicard, a selective β1‑adrenergic antagonist, is used in cardiovascular conditions that involve elevated blood pressure or impaired cardiac function.
  • Essential hypertension: reduces systolic and diastolic blood pressure to target levels.
  • Chronic heart failure: improves left ventricular ejection fraction and reduces hospitalization risk.
  • Hypertension with left ventricular dysfunction: provides blood pressure control while supporting cardiac performance.

How It Works

  • Nebivolol hydrochloride selectively blocks β1‑adrenergic receptors in cardiac tissue, decreasing heart rate and myocardial contractility. Concurrently, it stimulates endothelial nitric‑oxide synthase, leading to nitric‑oxide release and vasodilation of peripheral vessels. The combined effect lowers cardiac output and systemic vascular resistance, resulting in reduced arterial pressure and improved cardiac efficiency in heart‑failure patients.

Side Effects

Nebicard may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Fatigue: feeling of tiredness or reduced energy.
  • Headache: mild to moderate cranial pain.
  • Dizziness: sensation of light‑headedness, especially on standing.
  • Bradycardia: slower than normal heart rate.
  • Nausea: upset stomach or urge to vomit.

Serious or Rare Side Effects

  • Severe bradycardia: markedly low heart rate requiring medical attention.
  • Symptomatic hypotension: significant drop in blood pressure causing faintness.
  • Bronchospasm: tightening of airway muscles, particularly in patients with asthma.
  • Heart block: impaired electrical conduction in the heart.
  • Allergic reactions: rash, swelling, or anaphylaxis.

Precautions & Warnings

When prescribing Nebicard, clinicians should consider several safety measures to minimise risk.

  • Blood pressure monitoring: check baseline and periodic readings.
  • Cardiac function assessment: evaluate heart rate and ECG before initiation.
  • Concomitant beta‑blocker use: avoid combining with other β‑blockers or non‑selective agents.
  • Respiratory disease caution: use carefully in patients with asthma or COPD.
  • Renal/hepatic impairment: dose may need adjustment in reduced clearance.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture.

Avoid Interactions

Nebicard can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Other beta‑blockers: additive cardiac depression.
  • Calcium channel blockers verapamil or diltiazem: increased risk of AV‑block and bradycardia.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): raise nebivolol plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate hypotensive effect.
  • ACE inhibitors or ARBs: combined use can enhance blood pressure lowering.

Frequently Asked Questions

Nebicard contains nebivolol hydrochloride, a selective β1‑adrenergic antagonist indicated for the treatment of essential hypertension and chronic heart failure. It helps lower blood pressure and improves cardiac function in patients with reduced ejection fraction, under medical supervision.

Nebivolol works by selectively blocking β1‑adrenergic receptors in the heart, which reduces heart rate and contractility, while simultaneously stimulating endothelial nitric‑oxide synthase to cause vasodilation. This dual action decreases cardiac output and peripheral resistance, leading to lowered arterial pressure and enhanced cardiac efficiency.

The dosage of Nebicard is individualized; a qualified prescriber determines the appropriate strength and regimen based on the patient’s blood pressure, heart‑failure status, age, renal function and concomitant therapies. Patients should follow the prescribing information and not adjust the dose without medical advice.

Safety data for nebivolol during pregnancy and lactation are limited, and the product is generally classified as contraindicated or to be used only if the potential benefit outweighs the risk. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To request Nebicard, 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.

Compared with non‑selective beta‑blockers, nebivolol offers additional nitric‑oxide‑mediated vasodilation, which may improve endothelial function and cause fewer metabolic side effects. It is often considered alongside ACE inhibitors, ARBs or calcium‑channel blockers, with choice guided by patient comorbidities and tolerability.

Nebicard tablets should be stored at ambient temperature, below 25 °C, in the original blister or bottle, protected from moisture and direct sunlight. Keep the product out of reach of children and do not use after the expiration date.

Nebicard is taken orally, usually once daily, with or without food, as directed by the prescribing clinician. The tablet should be swallowed whole with a glass of water; it should not be crushed, chewed, or split unless specifically instructed.

The most serious adverse events include severe bradycardia, symptomatic hypotension, heart block, bronchospasm in patients with reactive airway disease, and rare allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience fainting, rapid heartbeat changes, difficulty breathing, or swelling.

Nebicard 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 or severe asthma/COPD. It should also be used with caution in patients with hepatic or renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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