Sparsentan bulk supplier for pharma manufacturers

Sparsentan Suppliers & Bulk Manufacturers

Available Forms: Tablets

Available Strengths: 200mg, 400mg

Reference Brands: Filspari (USA)

Category: Nephrology

Sparsentan is an oral dual endothelin type A receptor (ET_A) and angiotensin II type 1 receptor (AT_1) antagonist, designed to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) who are at risk of rapid disease progression. It is marketed under the brand name Filspari and available in 200 mg and 400 mg tablets. Because of its novel mechanism and risk profile (including hepatotoxicity), it is subject to a restricted drug-distribution program. Sparsentan is available in Tablets and strengths such as 200mg, 400mg. 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, Sparsentan 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)

Sparsentan 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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Frequently Asked Questions

Sparsentan is used to treat rare kidney diseases such as IgA nephropathy and focal segmental glomerulosclerosis (FSGS). It helps reduce proteinuria (excess protein in the urine) and slows the progression of kidney damage. Sparsentan works by blocking two key pathways involved in kidney injury — endothelin type A and angiotensin II type 1 receptors — offering dual protection to the kidneys.

Sparsentan is made from the active ingredient sparsentan, a dual-acting angiotensin II and endothelin receptor antagonist. Its chemical name is (2E)-3-[2-butyl-1-[(4′-carboxy[1,1′-biphenyl]-4-yl)methyl]-7-(2-methylpropyl)-2,6-dioxo-1,5-dihydro-4H-pyrrolo[3,2-d]pyrimidin-4-yl]-N-(2-hydroxy-2-phenylethyl)acrylamide. It is formulated with excipients such as lactose monohydrate, cellulose, and magnesium stearate depending on the dosage form.

The trade name of sparsentan is Filspári in the United States and Kinpeygo in the European Union.

Sparsentan (Filspári/Kinpeygo) is developed and marketed by Travere Therapeutics in the United States and by CSL Vifor in Europe under a licensing agreement.

The generic name of the drug is sparsentan.

The brand names of sparsentan are Filspári (USA) and Kinpeygo (EU).

Sparsentan is manufactured in the United States by Travere Therapeutics and in Europe by CSL Vifor, with global distribution to markets where treatment for IgA nephropathy and FSGS is approved.

Yes, Sparsentan 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, Sparsentan 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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