Fludarabine Phosphate Suppliers & Bulk Manufacturers
Available Forms: Injection (IV), Oral Tablet
Available Strengths: Injection: 25 mg/ml; Tablet: 10 mg
Reference Brands: Fludara® (US & EU)
Category: Oncology Cancer Care
Fludarabine Phosphate is an oncology drug used to treat CLL and blood cancers. Available as a 25 mg/mL IV injection and 10 mg tablets in the US and EU.
Product Description: Fludarabine Phosphate is a widely used oncology medication indicated for chronic lymphocytic leukemia (CLL) and certain non-Hodgkin’s lymphomas. It is available in the US and EU as a 25 mg/mL injection and 10 mg oral tablets. Marketed under the brand name Fludara® and as generics, Fludarabine Phosphate is a purine analog that interferes with DNA synthesis, promoting apoptosis in malignant cells. It is a critical chemotherapy option in hematologic cancer protocols and widely used in hospital oncology units and pharma B2B distribution. Its established efficacy and regulatory approval make it a trusted choice across global markets.
Fludarabine Phosphate — third party manufacturing & bulk supply
Fludarabine Phosphate 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
Manufacturers of Fludarabine Phosphate 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 Fludarabine Phosphate →The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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