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Mirikizumab-mrkz bulk supplier for pharma manufacturers

Mirikizumab-Mrkz 100 mg Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 100 mg

Reference Brands: Omvoh (USA)

Category: Immune Disorder

Mirikizumab-Mrkz is a Immune Disorder product available as Injection in strengths 100 mg. It corresponds to the reference brand Omvoh (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:

Mirikizumab‑MRKZ, marketed under the brand name Omvoh, is a monoclonal antibody approved for the treatment of moderately to severely active ulcerative colitis in adults. It works by selectively binding to interleukin-23 (IL-23), a cytokine involved in immune-mediated inflammation, and blocking its activity. This targeted mechanism helps reduce inflammation in the gastrointestinal tract and supports mucosal healing, offering a precision-based approach to managing ulcerative colitis.

Administered via subcutaneous injection, Omvoh is designed for patients who have not responded adequately to conventional therapies. The therapy provides a focused immunomodulatory effect while minimizing broader systemic immunosuppression. Patients receiving Omvoh should be monitored for potential adverse events, which most commonly include upper respiratory tract infections, headache, rash, and injection-site reactions. Its development and production are overseen by Eli Lilly and Company in clinical-grade facilities to ensure high-quality manufacturing and safety standards.

Omvoh represents an important therapeutic option in the management of ulcerative colitis, providing targeted disease control and improving patient quality of life through a novel mechanism of action.

Mirikizumab-Mrkz — third party manufacturing & bulk supply

Mirikizumab-Mrkz 100 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 Mirikizumab-Mrkz 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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Disclaimer: By continuing to browse, you agree to the terms of use of this website and the Trade Marks displayed, in compliance with the provisions of the Trademark Act, 1999, Section 30 and 30(1) under 'Fair use.'

The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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Frequently Asked Questions


It is used for the treatment of moderately to severely active ulcerative colitis and Crohn’s disease in adults who have inadequate response to conventional therapies.


It is a humanized monoclonal antibody that selectively binds to interleukin-23 (IL-23), inhibiting inflammatory pathways.


It does not have a trade name in this section (see brand name below).


Eli Lilly and Company.


The generic name is mirikizumab‑MRKZ.


Omvoh (USA).


It is manufactured in clinical-grade facilities under Eli Lilly oversight for research, clinical trials, and commercial distribution.

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