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Selexipag bulk supplier for pharma manufacturers

Selexipag Suppliers & Bulk Manufacturers

Available Forms: Tablets / Injection

Available Strengths: 200 mcg, 400 mcg, 600 mcg, 800 mcg, 1000 mcg, 1200 mcg, 1400 mcg, 1600 mcg

Reference Brands: Uptravi (USA/EU)

Category: Heart Disorder

Selexipag is available in Tablets / Injection and strengths such as 200 mcg, 400 mcg, 600 mcg, 800 mcg, 1000 mcg, 1200 mcg, 1400 mcg, 1600 mcg. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Selexipag is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.

Technical Specifications & Supply Details
Lead Time 7 to 60 days (depending on batch size & schedule)
MOQ As per manufacturer’s batch size
COA Available with every batch
Regulatory Dossier / DMF Available upon request
Export Documentation FSC, COA, Manufacturing License, Product Permission
Standards IP, BP, USP
Certifications WHO-GMP, EU-GMP, USFDA (as applicable)

Selexipag can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.

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📘 Sourcing Guide

Product Description:

Selexipag is a selective prostacyclin (IP) receptor agonist indicated for the long-term treatment of pulmonary arterial hypertension (PAH). It is used to delay disease progression and reduce the risk of hospitalization associated with PAH. Developed by Actelion, Selexipag represents an advanced, non-prostanoid therapeutic option that targets the prostacyclin pathway, a key mechanism involved in pulmonary vascular remodeling and increased pulmonary arterial pressure.

After oral or intravenous administration, Selexipag is rapidly metabolized into its active metabolite, ACT-333679 (also known as MRE-269), which exhibits a high affinity for the prostacyclin receptor. Activation of this receptor leads to vasodilation of the pulmonary arteries, inhibition of smooth muscle cell proliferation, and improved pulmonary blood flow. Unlike traditional prostacyclin analogues, Selexipag offers targeted receptor activity with a more convenient dosing profile.

Selexipag can be administered as oral tablets for chronic therapy or intravenously for patients who are temporarily unable to take oral medication. It is commonly used as monotherapy or in combination with other PAH treatments, including endothelin receptor antagonists and phosphodiesterase-5 inhibitors, making it a valuable option in comprehensive PAH management strategies.

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Frequently Asked Questions

Selexipag is used for the treatment of pulmonary arterial hypertension (PAH) to delay disease progression and reduce the risk of hospitalization related to PAH.

Selexipag is a chemically synthesized small-molecule drug that acts as a selective agonist of the prostacyclin (IP) receptor.

The trade name of Selexipag is Uptravi.

Selexipag (Uptravi) is manufactured and marketed by Actelion Pharmaceuticals Ltd., a Janssen Pharmaceutical company.

The generic name of Uptravi is Selexipag.

The brand name of Selexipag is Uptravi.

Selexipag is manufactured at Actelion/Janssen approved pharmaceutical manufacturing facilities, primarily located in Europe and the United States, in compliance with international regulatory standards.

Yes, Selexipag is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Selexipag is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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