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Ibutilide Fumarate bulk supplier for pharma manufacturers

Ibutilide Fumarate 0.1 mg /ml Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 0.1 mg /ml

Reference Brands: Corvert (USA)

Category: Heart Disorder

Ibutilide Fumarate is a Heart Disorder product available as Injection in strengths 0.1 mg /ml. It corresponds to the reference brand Corvert (USA). Verified GMP manufacturers and suppliers on PharmaTradz offer it in bulk for import worldwide, with regulatory documentation and dossier support available on request.

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📘 Sourcing Guide

Product Description:

Ibutilide fumarate is a Class III antiarrhythmic agent indicated for the acute cardioconversion of atrial fibrillation and atrial flutter of recent onset to normal sinus rhythm. Marketed under the brand name Corvert, it is administered intravenously under strict medical supervision in a hospital setting.

Ibutilide exerts its antiarrhythmic effect by inducing a slow inward sodium current, which prolongs the action potential duration and refractory period of myocardial cells. This mechanism helps restore and maintain normal cardiac rhythm in patients experiencing recent-onset atrial arrhythmias. Due to its potent Class III antiarrhythmic activity, ibutilide must not be administered concomitantly with other Class Ia or Class III antiarrhythmic agents, as this may increase the risk of proarrhythmia.

Its intravenous formulation allows precise dosing and rapid therapeutic action, making it a critical intervention for acute management of atrial fibrillation and atrial flutter. Ibutilide fumarate remains an essential tool in cardiology for achieving timely rhythm control while monitoring for potential cardiac adverse events during treatment.

Ibutilide Fumarate — third party manufacturing & bulk supply

Ibutilide Fumarate 0.1 mg /ml is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.
Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.
Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

What to include when you enquire

  • Destination market — determines which manufacturers hold the right site-level approvals
  • First order quantity and estimated annual volume
  • Whether you need a registration dossier or the product is already registered
  • Packaging, labelling and language requirements
  • Incoterms and required shelf life

Manufacturers of Ibutilide Fumarate listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding. Narcotic drugs and controlled substances are supplied strictly against valid import and export permits issued by the competent authorities.

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Frequently Asked Questions


Ibutilide fumarate is used for the acute conversion of atrial fibrillation or atrial flutter to normal sinus rhythm in adult patients. It is administered intravenously under medical supervision in a hospital setting.


Ibutilide fumarate is a synthetic class III antiarrhythmic agent that works by prolonging the action potential duration and refractory period in cardiac cells, helping restore normal heart rhythm.


Ibutilide fumarate is marketed under the trade name Corvert.


Ibutilide fumarate (Corvert) is manufactured by multiple pharmaceutical companies, including Pfizer in the USA, depending on regional regulatory approvals.


The generic name of the product is ibutilide fumarate.


A commonly recognized brand name of ibutilide fumarate is Corvert.


Ibutilide fumarate is manufactured in various countries including the USA and EU regions, depending on the approved manufacturer and market authorization.

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