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Ensifentrine bulk supplier for pharma manufacturers

Ensifentrine 3 mg per 2.5 mL Suppliers & Bulk Manufacturers

Available Forms: Inhalation solution

Available Strengths: 3 mg per 2.5 mL

Reference Brands: Ohtuvayre (USA)

Category: Respiratory Disorder

Ensifentrine is a nebulised maintenance treatment for chronic obstructive pulmonary disease (COPD), the first to block both PDE3 and PDE4, which relaxes the airways and reduces inflammation. It was approved in the US in 2024 as Ohtuvayre and is still a patented innovator product. Supply is through authorised distribution or named-patient import; ask us which route fits your country.

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Product Description:

Ensifentrine is an inhaled medication used for the maintenance treatment of chronic obstructive pulmonary disease (COPD) in adults. It is marketed under the brand name Ohtuvayre and represents a novel therapeutic approach by combining dual inhibition of phosphodiesterase 3 (PDE3) and phosphodiesterase 4 (PDE4) in a single molecule. This dual mechanism allows ensifentrine to deliver both bronchodilator and anti-inflammatory effects, addressing key pathological features of COPD.

As a PDE3 inhibitor, ensifentrine helps relax airway smooth muscle, leading to bronchodilation and improved airflow. At the same time, its PDE4 inhibitory activity reduces airway inflammation, which contributes to symptom control and disease management. Ensifentrine is administered by inhalation, allowing targeted delivery directly to the lungs and minimizing systemic exposure.

Ensifentrine is indicated for long-term COPD management and is used to improve lung function and reduce respiratory symptoms. Its inhaled formulation makes it suitable for patients who require consistent, localized therapy. By combining bronchodilation and anti-inflammatory action in one treatment, ensifentrine offers a differentiated and effective option for personalized respiratory care in adult COPD patients.

How Ensifentrine is supplied today, and licensing ahead of patent expiry

Named-patient import Where a patient needs the product in a market where it is not registered, named-patient import is the lawful route. It requires the treating physician's documentation and authorisation from the destination regulator. We handle this pathway. Named-patient access
Authorised distribution For registered markets, supply runs through the manufacturer's authorised distribution channel. We can identify the authorised route for your market and tell you whether the product is registered there at all. Innovator sourcing
A genericised alternative Where the clinical requirement is the drug class rather than this specific molecule, there is often an off-patent alternative that is faster to register and materially cheaper. Tell us the indication and target market and we will say plainly whether one exists. Discuss alternatives
Licensing and generic development Patents expire country by country, and in many countries development and dossier filing can start before expiry under research and regulatory-review exemptions. We connect manufacturers developing this molecule, dossier holders, licensees and tech-transfer partners for markets where it is, or will become, off-patent. Partner on this molecule
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Frequently Asked Questions


Ensifentrine is used for the maintenance treatment of chronic obstructive pulmonary disease (COPD) in adults. It helps improve lung function and reduce respiratory symptoms associated with COPD.


Ensifentrine is a small-molecule, dual phosphodiesterase (PDE) inhibitor that selectively inhibits PDE3 and PDE4 enzymes involved in airway inflammation and bronchoconstriction.


The trade name of ensifentrine is Ohtuvayre.


Ensifentrine is developed and marketed by Verona Pharma.


The generic name is ensifentrine.


The brand name is Ohtuvayre.


Ensifentrine is manufactured in GMP-compliant pharmaceutical facilities for commercial supply in the United States.

As 3 mg nebulised twice daily through a standard jet nebuliser, on top of other COPD maintenance inhalers.

No. It was approved by the FDA in June 2024 as Ohtuvayre (Verona Pharma, now part of Merck) and remains under patent.

Through named-patient or special import routes until it is registered locally.

Ohtuvayre (Ensifentrine) is developed and sold by Verona Pharma (Merck & Co). PharmaTradz handles enquiries for authorised supply of the originator product, named-patient import where it is not registered, and licensing or development work ahead of patent expiry.

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