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Ferric Carboxymaltose API Suppliers & Bulk Manufacturers

Available Forms: API (drug substance)

Available Strengths: USP grade or in-house specification

Reference Brands: Injectafer, Ferinject

Category: Active Pharmaceutical Ingredient

Ferric carboxymaltose is an iron-carbohydrate complex given intravenously for iron deficiency. Injectable formulation makers and CDMOs source this complex drug substance.

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Product Description:

Ferric carboxymaltose is a colloidal complex of a polynuclear iron(III) hydroxide core with a carboxymaltose carbohydrate ligand, which releases iron gradually for uptake into the body's iron stores. It is approved for iron deficiency anaemia when oral iron is not tolerated or has not worked, for iron deficiency anaemia in non-dialysis chronic kidney disease, and for iron deficiency in adults with NYHA class II/III heart failure to improve exercise capacity (reference brand: Injectafer, Ferinject).

Specification at a glance

Traded formNon-biological complex drug: polynuclear iron(III) hydroxide core with a carboxymaltose ligand.
CAS number9007-72-1
Molecular formula[FeOx(OH)y(H2O)z]n[{(C6H10O5)m(C6H12O7)}l]k (n ≈ 103, m ≈ 8, l ≈ 11, k ≈ 4)
Molecular weightapprox. 150,000 Da (relative)
PharmacopoeiaNo official monograph found; USP listed ferric carboxymaltose as a priority new monograph in 2024 (status unverified). Otherwise supplied to an in-house specification.

Regulatory files and timing

The FDA list of Drug Master Files (third quarter 2026) shows 16 active Type II API DMFs for this molecule. There is a fair choice of sources, so compare documents and impurity profiles, not just price. For Europe, ask whether the supplier holds a CEP or an EU ASMF and, for imports into the EU, a written confirmation.

Generic or biosimilar entry. United States: Generics/biosimilars on the market (Jul 2026). European Union: No confirmed date.

Handling and quality points

Ferric carboxymaltose is a complex drug rather than a single molecule, so sameness rests on physicochemical characterisation: molecular weight distribution, iron core size and structure, labile iron, and carbohydrate content. EMA and FDA set out specific expectations for iron-carbohydrate products, and buyers should ask how the supplier's material compares with the reference product on these points. Endotoxin, bioburden and elemental impurity data are needed because the product is given intravenously.

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Brand names are trademarks of their respective owners and identify the reference medicine only. Information is general and was checked in October 2026; confirm specifications and filings with the supplier before purchase.

Ferric Carboxymaltose API — third party manufacturing & bulk supply

Ferric Carboxymaltose API 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:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.
Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.
Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

Indicative minimum order quantity

Ferric Carboxymaltose API is supplied as API (drug substance) — a dosage form priced by order value, so the indicative MOQ is a minimum order value of USD 5,000 per product. 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 Ferric Carboxymaltose API listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.

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Frequently Asked Questions

A GMP certificate, specification and CoA, and a US DMF letter of access or EU ASMF, are the base. Because this is a complex drug, also ask for a full physicochemical characterisation package compared with the reference product, plus stability, endotoxin and elemental impurity data.

As a non-biological complex drug, it needs a side-by-side physicochemical comparison with the reference product rather than simple chemical identity. Regulators expect tests such as iron core characterisation, molecular weight distribution and labile iron, and may ask for further non-clinical or clinical data, so check FDA and EMA guidance for your market early.

Yes. PharmaTradz links licensed manufacturers, CDMOs and R&D teams with GMP-compliant producers of ferric carboxymaltose and checks their documentation before an introduction. Your company stays anonymous until both sides agree.

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