Gemcitabine 200 mg, 1000 mg, 1500 mg Suppliers & Bulk Manufacturers
Available Forms: Lyophilized powder for solution for injection/infusion
Available Strengths: 200 mg, 1000 mg, 1500 mg
Reference Brands: Gemzar® (US & EU)
Category: Oncology Cancer Care
Gemcitabine is an FDA- and EMA-approved oncology drug used to treat various cancers, including lung, pancreatic, and breast cancer. Available in 200 mg, 1 g, and 1.5 g vials for IV infusion, it is widely supplied across the US and EU pharmaceutical B2B markets. Reliable sourcing and quality assurance make it a key chemotherapy product for hospitals and clinics.
Product Description: Gemcitabine is a widely used oncology chemotherapy drug available in both the US and EU pharmaceutical B2B markets. Offered in 200 mg, 1 g, and 1.5 g vials, Gemcitabine comes as a lyophilized powder for intravenous infusion. Trusted by hospitals and oncology centers, it is essential for treating cancers such as pancreatic, lung, bladder, and breast cancer. Approved by the FDA and EMA, Gemcitabine is available through certified pharmaceutical wholesalers and B2B distributors across Europe and the United States. Buyers seeking reliable Gemcitabine suppliers can access competitive pricing, consistent quality, and regulatory-compliant sourcing for hospital and clinical use.
Gemcitabine — third party manufacturing & bulk supply
Gemcitabine 200 mg, 1000 mg, 1500 mg 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:
Indicative minimum order quantity
Gemcitabine is supplied as Lyophilized powder for solution for injection/infusion — an injectable dosage form, so the indicative MOQ is 50,000 units. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.
Manufacturers of Gemcitabine listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
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