Product image of Nebivolol Crescent Pharma (Nebivolol Hydrochloride) supplied by GNH India

Nebivolol Crescent Pharma

Active Ingredient:
Nebivolol Hydrochloride
Origin:
EU

Nebivolol Crescent Pharma (Nebivolol Hydrochloride)

Nebivolol, the active ingredient in Nebivolol Crescent Pharma, is a selective β1‑adrenergic antagonist presented as an oral tablet for oral use. It is used to lower elevated blood pressure in adults with hypertension.

GNH India supplies Nebivolol Crescent Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Crescent Pharma Limited

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Indications & Clinical Uses

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

  • Essential hypertension: reduces systolic and diastolic pressure by decreasing heart rate and peripheral resistance.
  • Stage 1 hypertension: helps achieve target blood pressure when lifestyle measures are insufficient.
  • Stage 2 hypertension: provides additional blood‑pressure control in patients requiring more intensive therapy.

How It Works

  • Nebivolol selectively blocks β1‑adrenergic receptors on cardiac myocytes, lowering heart rate and contractility. In parallel, it stimulates endothelial nitric‑oxide synthase, causing nitric‑oxide‑mediated vasodilation that reduces peripheral vascular resistance, together resulting in lowered arterial pressure.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate discomfort.
  • Dizziness or light‑headedness, especially on standing.
  • Fatigue or general tiredness.
  • Nasal congestion or rhinorrhea.
  • Peripheral edema: mild swelling of ankles or feet.
  • Bradycardia: slower than normal heart rate.

Serious or Rare Side Effects

  • Severe bradycardia or heart block requiring medical attention.
  • Acute bronchospasm in patients with reactive airway disease.
  • Hepatic dysfunction manifested by elevated liver enzymes.
  • Allergic reactions such as rash, pruritus, or angio‑edema.
  • Syncope or fainting episodes.
  • Cardiogenic shock in extreme cases.

Precautions & Warnings

Before initiating Nebivolol, clinicians should evaluate patient‑specific risk factors and monitor therapy.

  • Cardiovascular assessment: review heart rate, rhythm, and any history of heart block.
  • Renal impairment: adjust monitoring if creatinine clearance is reduced.
  • Hepatic disease: use caution in patients with liver dysfunction.
  • Concomitant beta‑blockers: avoid additive effects that may cause excessive bradycardia.
  • Pregnancy and lactation: prescribe only if benefits outweigh potential risks.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Nebivolol may interact with other medicines that affect heart rate, blood pressure, or drug metabolism.

Major Interactions (Avoid)

  • Other beta‑blockers: risk of profound bradycardia and hypotension.
  • Calcium‑channel blockers (verapamil, diltiazem): can increase plasma concentrations of nebivolol.
  • Strong CYP2D6 inhibitors (e.g., paroxetine, quinidine): may raise nebivolol levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate antihypertensive effect, requiring blood‑pressure checks.
  • ACE inhibitors or ARBs: combined therapy can enhance blood‑pressure lowering.
  • NSAIDs: may blunt antihypertensive response.
  • Antidiabetic agents: monitor glucose as beta‑blockade can mask hypoglycaemia signs.

Frequently Asked Questions

Nebivolol Crescent Pharma is prescribed to treat hypertension. By lowering heart rate and relaxing blood vessels, it helps achieve and maintain target blood‑pressure levels in adult patients diagnosed with elevated systolic or diastolic pressure.

Nebivolol selectively blocks β1‑adrenergic receptors on the heart, reducing heart rate and contractile force. At the same time, it enhances nitric‑oxide release from the endothelium, causing vasodilation and decreasing peripheral vascular resistance, which together lower arterial pressure.

The appropriate dose of nebivolol is determined by the prescribing clinician based on the individual’s medical condition, response to therapy, and any co‑existing health issues. Patients should follow the dosage instructions provided on the prescription label.

Nebivolol should be used during pregnancy or lactation only if the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers typically evaluate alternative therapies first, and women who are pregnant or nursing should discuss risks with their doctor.

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 distinguished by its combined β1‑blockade and nitric‑oxide‑mediated vasodilation, which can result in fewer metabolic side effects compared with non‑vasodilating beta‑blockers. It may be preferred when clinicians seek both heart‑rate control and additional vascular relaxation.

Nebivolol tablets should be stored at ambient 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 once daily with or without food, as directed by the prescribing physician. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious adverse events include severe bradycardia, heart block, bronchospasm in patients with reactive airway disease, and rare cases of hepatic dysfunction or allergic reactions such as angio‑edema. Patients should seek immediate medical attention if they experience fainting, severe shortness of breath, or signs of an allergic reaction.

Nebivolol is contraindicated in patients with known hypersensitivity to the drug, those with severe bradycardia, second‑ or third‑degree atrioventricular block without a pacemaker, and individuals with uncompensated heart failure. Clinicians should also exercise caution in patients with asthma or chronic obstructive pulmonary disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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