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Quizartinib Dihydrochloride bulk supplier for pharma manufacturers

Quizartinib Dihydrochloride Suppliers & Bulk Manufacturers

Available Forms: Tablets

Available Strengths: 17.7 mg , 26.5 mg

Reference Brands: Vanflyta (USA/EU)

Category: Oncology Cancer Care

Quizartinib Dihydrochloride is available in Tablets and strengths such as 17.7 mg , 26.5 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, Quizartinib Dihydrochloride 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)

Quizartinib Dihydrochloride 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:

Quizartinib dihydrochloride is a targeted anticancer therapy used in the treatment of acute myeloid leukemia (AML), particularly in patients whose disease carries a mutation in the FMS-like tyrosine kinase 3 (FLT3) gene. AML is a rapidly progressing hematologic malignancy characterized by the uncontrolled growth of immature myeloid cells in the bone marrow and blood. Advances in molecular research have identified several genetic mutations that play a role in the development and progression of AML, with FLT3 mutations being among the most common and clinically significant targets for therapy.

Quizartinib is a second-generation FLT3 inhibitor designed to selectively block the activity of the FLT3 receptor tyrosine kinase. By inhibiting this abnormal signaling pathway, the drug helps reduce the proliferation of leukemia cells and supports better disease control when used as part of combination treatment strategies. Compared to earlier FLT3 inhibitors, quizartinib was developed to provide more targeted and potent inhibition of the FLT3 mutation.

The medicine is available in oral tablet form and is typically used in combination with standard chemotherapy for patients with newly diagnosed FLT3-ITD positive AML, followed by maintenance therapy. Quizartinib represents an important advancement in precision oncology, offering a mutation-directed treatment approach that helps improve outcomes in patients with specific genetic profiles of AML.

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Frequently Asked Questions

Quizartinib dihydrochloride is used for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) that is FLT3-ITD positive. It is usually given in combination with standard chemotherapy during induction and consolidation therapy and may also be used as maintenance treatment to help reduce the risk of disease relapse.

Quizartinib dihydrochloride is a synthetic small-molecule targeted therapy designed to selectively inhibit the FLT3 (FMS-like tyrosine kinase 3) receptor. By blocking this receptor, the medicine helps slow or stop the growth of leukemia cells that carry the FLT3 mutation.

The main trade name of quizartinib dihydrochloride is Vanflyta.

Vanflyta (quizartinib dihydrochloride) is developed and marketed by Daiichi Sankyo.

The generic name of Vanflyta is quizartinib dihydrochloride.

The well-known brand name of quizartinib dihydrochloride is Vanflyta.

Quizartinib dihydrochloride products such as Vanflyta are manufactured in GMP-certified pharmaceutical manufacturing facilities that are part of the global supply network of Daiichi Sankyo and its approved partners.

Yes, Quizartinib Dihydrochloride 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, Quizartinib Dihydrochloride 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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