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Histrelin Acetate bulk supplier for pharma manufacturers

Histrelin Acetate 50 mg Suppliers & Bulk Manufacturers

Available Forms: Subcutaneous implant

Available Strengths: 50 mg

Reference Brands: Vantas (USA), Supprelin LA (USA)

Category: Oncology Cancer Care

Histrelin Acetate is a Oncology Cancer Care product available as Subcutaneous implant in strengths 50 mg. It corresponds to the reference brands Vantas (USA), Supprelin LA (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:

Histrelin acetate is a synthetic gonadotropin-releasing hormone (GnRH) agonist used in hormone-based therapy for certain endocrine and hormone-dependent conditions. It is used as palliative treatment for advanced prostate cancer and for the management of central precocious puberty in children. Histrelin acetate works by initially stimulating the pituitary gland to release luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which may briefly increase sex hormone levels. With continuous exposure, it suppresses LH and FSH secretion, resulting in a significant reduction in testosterone in males and estrogen in females.

This hormone suppression effect makes it useful in androgen deprivation therapy for prostate cancer and in controlling early onset puberty. Histrelin acetate is marketed under brand names such as Vantas for prostate cancer care and Supprelin LA for pediatric endocrine use. It is designed for long-acting delivery to provide sustained hormonal control over an extended period. Treatment is typically managed by specialists with regular monitoring of hormone levels and clinical response to ensure effective and safe therapy outcomes.

Histrelin Acetate — third party manufacturing & bulk supply

Histrelin Acetate 50 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 Histrelin Acetate 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

Histrelin acetate is used for the treatment of advanced prostate cancer and for central precocious puberty in children.

It is a synthetic gonadotropin-releasing hormone (GnRH) agonist peptide formulated as the acetate salt for long-acting implant delivery.

The trade names are Vantas and Supprelin LA.

It is marketed by Endo Pharmaceuticals and related specialty pharma companies depending on the brand and region.

The generic name is histrelin acetate.

The brand names are Vantas and Supprelin LA.

It is manufactured in regulated pharmaceutical facilities compliant with US and international GMP standards by licensed manufacturers for the marketing companies.

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