Sirolimus Tablet Suppliers & Bulk Manufacturers
Available Forms: Tablet
Available Strengths: 1 mg, 2 mg, 3 mg, 5 mg tablets
Reference Brands: Rapamune(US)
Category:
Immune Disorder
Sirolimus inhibits mTOR, blocking T-cell activation and proliferation. It reduces organ rejection in transplant patients and treats certain autoimmune diseases. Benefits include effective immunosuppression, decreased rejection risk, and improved graft survival. Its selectivity for immune cells supports long-term disease control with manageable side effects.
Sirolimus tablet is available in Tablet
and strengths such as 1 mg, 2 mg, 3 mg, 5 mg tablets.
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, Sirolimus tablet 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) |
Sirolimus tablet 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.
Product Description:
Sirolimus tablets, marketed as Rapamune, are approved in the US by the FDA and in the EU via EMA for preventing organ rejection and treating certain autoimmune conditions. Regulatory approval requires a comprehensive dossier including clinical efficacy, safety, manufacturing data, and pharmacovigilance plans. In the US, the FDA reviews detailed clinical trial and manufacturing information, while the EMA ensures compliance with regional standards. For guidance on dossier preparation, regulatory pathways, and market access strategies, visit PharmaTradz. Ensuring adherence to regional regulations is essential for the safe, effective, and timely approval of sirolimus tablets worldwide, supporting optimal patient outcomes in transplantation and autoimmune therapy.
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