Rolapitant Hydrochlorid 90 mg Suppliers & Bulk Manufacturers
Available Forms: Tablets
Available Strengths: 90 mg
Reference Brands: Varubi(USA/LATAM), Varuby(EU)
Category: Critical Care
Rolapitant Hydrochlorid is a Critical Care product available as Tablets in strengths 90 mg. It corresponds to the reference brands Varubi(USA/LATAM), Varuby(EU). Verified GMP manufacturers and suppliers on PharmaTradz offer it in bulk for import worldwide, with regulatory documentation and dossier support available on request.
Product Description:
Rolapitant hydrochloride is an orally administered, selective neurokinin-1 (NK1) receptor antagonist with potent antiemetic activity, primarily used to prevent chemotherapy-induced nausea and vomiting (CINV) in adult patients receiving moderately or highly emetogenic cancer therapy. The drug works by competitively binding to NK1 receptors in the central nervous system, thereby blocking the activity of substance P, a key neuropeptide responsible for triggering nausea and vomiting. By inhibiting this pathway, rolapitant helps prevent both acute and delayed emesis associated with cancer chemotherapy.
Rolapitant distinguishes itself from other NK1 receptor antagonists through its rapid onset of action and extended half-life, allowing for effective, long-lasting protection against CINV with a single oral dose. It is typically administered in combination with other antiemetic agents, such as 5-HT3 receptor antagonists and corticosteroids, to maximize patient comfort and adherence to cancer treatment regimens.
As a centrally acting antiemetic, rolapitant provides an important supportive care option for oncology patients, improving quality of life during chemotherapy by reducing the burden of nausea and vomiting and allowing patients to better tolerate their prescribed cancer therapy.
Rolapitant Hydrochlorid — third party manufacturing & bulk supply
Rolapitant Hydrochlorid 90 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:
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
Indicative minimum order quantity
Rolapitant Hydrochlorid is supplied as Tablets — an oral solid dosage form, so the indicative MOQ is 200,000 units. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.
Manufacturers of Rolapitant Hydrochlorid 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.
Request a quote for Rolapitant Hydrochlorid →The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Frequently Asked Questions
Rolapitant hydrochloride is used to prevent delayed nausea and vomiting caused by moderately or highly emetogenic chemotherapy in adults. It is given in combination with other antiemetic medications to improve patient comfort and adherence to cancer treatment.
Rolapitant hydrochloride is a synthetic small-molecule NK1 receptor antagonist that blocks the binding of substance P, a neuropeptide involved in triggering nausea and vomiting, to the NK1 receptor in the central nervous system.
Common trade names include Varubi (USA) and Varuby (EU).
Varubi (rolapitant hydrochloride) is marketed by Tesaro (a GSK company).
The generic name of Varubi is rolapitant hydrochloride.
Well-known brand names are Varubi and Varuby.
Rolapitant hydrochloride tablets are manufactured in GMP-certified pharmaceutical facilities approved for oncology medications, primarily in the USA and Europe, following strict quality and safety standards.
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