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Momelotinib bulk supplier for pharma manufacturers

Momelotinib 100 mg, 150 mg, 200 mg Suppliers & Bulk Manufacturers

Available Forms: Tablets

Available Strengths: 100 mg, 150 mg, 200 mg

Reference Brands: Ojjaara (USA)

Category: Oncology Cancer Care

Momelotinib is a Oncology Cancer Care product available as Tablets in strengths 100 mg, 150 mg, 200 mg. It corresponds to the reference brand Ojjaara (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:

Momelotinib is an oral anticancer medication used for the treatment of myelofibrosis, a rare bone marrow disorder characterized by abnormal blood cell production, splenomegaly, and anemia. It is marketed under the brand name Ojjaara and belongs to the class of Janus kinase (JAK) inhibitors. Momelotinib works by inhibiting JAK1 and JAK2 signaling pathways involved in inflammation and abnormal cell proliferation, while also modulating pathways related to anemia, making it a differentiated therapy for patients with myelofibrosis.

Momelotinib is indicated for adult patients with intermediate or high-risk myelofibrosis, including primary myelofibrosis and secondary myelofibrosis arising from polycythemia vera or essential thrombocythemia. The medication is administered orally, offering convenience for long-term disease management.

Common adverse reactions associated with momelotinib therapy include dizziness, fatigue, diarrhea, nausea, thrombocytopenia, hemorrhage, and bacterial infections. Due to these potential effects, patients receiving momelotinib require regular clinical and laboratory monitoring. Overall, momelotinib provides an important targeted treatment option for managing myelofibrosis, particularly in patients with disease-related anemia, supporting improved symptom control and quality of life.

Momelotinib — third party manufacturing & bulk supply

Momelotinib 100 mg, 150 mg, 200 mg 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 Momelotinib 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


Momelotinib is used for the treatment of adult patients with intermediate or high-risk myelofibrosis, including primary myelofibrosis and secondary myelofibrosis following polycythemia vera or essential thrombocythemia. It is particularly beneficial for patients with anemia associated with myelofibrosis.


Momelotinib is a small-molecule kinase inhibitor that targets Janus kinase (JAK) 1 and 2 and activin A receptor type 1 (ACVR1), helping regulate inflammatory signaling and hepcidin production.


The trade name of momelotinib is Ojjaara.


Momelotinib is developed and marketed by GSK (GlaxoSmithKline).


The generic name is momelotinib.


The brand name is Ojjaara.


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

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