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Pasireotide Diaspartate bulk supplier for pharma manufacturers

Pasireotide Diaspartate Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 0.3 mg/mL, 0.6 mg/mL, 1.2 mg/mL, 10 mg, 20 mg, 30 mg

Reference Brands: Signifor (USA/EU)

Category: Orphan Drugs

Pasireotide Diaspartate is available in Injection and strengths such as 0.3 mg/mL, 0.6 mg/mL, 1.2 mg/mL, 10 mg, 20 mg, 30 mg. 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, Pasireotide Diaspartate 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)

Pasireotide Diaspartate 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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📘 Sourcing Guide

Product Description:

Pasireotide is an orphan drug used for the treatment of Cushing’s disease in patients who are not candidates for pituitary surgery or have persistent or recurrent disease following surgery. Marketed under the brand name Signifor, Pasireotide was developed by Novartis and has received approval in the United States and European Union for this rare endocrine disorder.

It is a synthetic somatostatin analogue with a uniquely high affinity for somatostatin receptor subtype 5, approximately 40 times greater than other somatostatin analogues. By selectively binding to this receptor, Pasireotide effectively inhibits excess adrenocorticotropic hormone (ACTH) secretion, leading to reduced cortisol production and helping restore hormonal balance in patients with Cushing’s disease.

Pasireotide is available in both short-acting subcutaneous formulations and long-acting intramuscular depot injections, offering flexibility in treatment schedules ranging from daily to monthly dosing. Due to its targeted mechanism of action, patients require monitoring for potential effects on glucose metabolism, liver function, and gallbladder health. As an orphan drug, Pasireotide provides a specialized therapeutic option for managing a rare and challenging endocrine condition.

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Frequently Asked Questions

Pasireotide diaspartate is used for the treatment of Cushing’s disease in patients not eligible for surgery or with persistent or recurrent disease, and in selected cases of acromegaly.

Pasireotide diaspartate is a synthetic somatostatin analogue designed to bind multiple somatostatin receptor subtypes to regulate hormone secretion.

The trade name of Pasireotide diaspartate is Signifor.

Pasireotide diaspartate (Signifor) is developed and marketed by Novartis Pharmaceuticals.

The generic name of Signifor is Pasireotide diaspartate.

The brand name of Pasireotide diaspartate is Signifor.

Pasireotide diaspartate is manufactured at Novartis-approved facilities under international GMP and regulatory standards.

Yes, Pasireotide Diaspartate 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, Pasireotide Diaspartate 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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