Lusutrombopag bulk supplier for pharma manufacturers

Lusutrombopag Suppliers & Bulk Manufacturers

Available Forms: Tablets

Available Strengths: 3 mg

Reference Brands: Mulpleta (USA), Mulpleo (EU)

Category: Blood Disorder

Lusutrombopag is an orally administered thrombopoietin receptor agonist used to treat thrombocytopenia (low platelet count) in adults with chronic liver disease who are scheduled for an invasive procedure. It stimulates bone marrow to produce more platelets, helping reduce bleeding risk. Lusutrombopag tablets are typically taken once daily for a short course before the scheduled procedure. The most common side effect reported is headache. It represents a targeted approach to safely elevate platelet counts before medical or dental procedures. Lusutrombopag is available in Tablets and strengths such as 3 mg. 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, Lusutrombopag 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)

Lusutrombopag 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:

Lusutrombopag is a small‑molecule thrombopoietin (TPO) receptor agonist that is used in adult patients with chronic liver disease who have thrombocytopenia (a low number of platelets) and are scheduled to undergo an invasive procedure. It helps stimulate the body’s bone marrow to increase the production of platelets by activating TPO receptors on megakaryocytes and their progenitor cells. This action increases circulating platelet counts, reducing the need for platelet transfusions and lowering the risk of excessive bleeding during or after surgical, dental, or diagnostic procedures. Lusutrombopag is provided in 3 mg oral tablet form, typically administered once daily with or without food for a duration of up to 7 days before the scheduled procedure. Treatment is usually started several days prior to the procedure and the procedure is performed shortly after the final dose. While generally well‑tolerated, common side effects include headache, and rare but serious risks include excessive platelet elevation or thromboembolic events, so monitoring is advised. Lusutrombopag is marketed under brand names such as Mulpleta in the USA and Mulpleo in the EU/UK, and its use has expanded as a non‑transfusion option to elevate platelet counts in high‑risk patients.

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Frequently Asked Questions

Lusutrombopag is used to treat thrombocytopenia (low platelet count) in adult patients with chronic liver disease who are scheduled to undergo an invasive procedure, to reduce the risk of bleeding.

Lusutrombopag is a synthetic small-molecule drug that acts as a thrombopoietin receptor agonist, stimulating platelet production in the bone marrow.

The main trade names for lusutrombopag are Mulpleta in the USA and Mulpleo in the EU/UK.

Lusutrombopag products such as Mulpleta and Mulpleo are manufactured and marketed under license by Shionogi & Co. and its affiliates in different regions.

The generic name of Mulpleta is lusutrombopag.

The brand names for lusutrombopag include Mulpleta (USA) and Mulpleo (EU/UK).

Lusutrombopag tablets are manufactured under regulated pharmaceutical conditions by companies authorized to produce and distribute them for their respective markets.

Yes, Lusutrombopag 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, Lusutrombopag 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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