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Brand-name prescription medicine

Feraheme

Generic name: Ferumoxytol (ferumoxytol non-stoichiometric magnetite)

FDA application holder: Azurity

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Feraheme?
Feraheme is a brand name of Ferumoxytol (ferumoxytol non-stoichiometric magnetite), a prescription medicine. The FDA NDC Directory lists 1 Feraheme product in 1 strength and form.
Who makes Feraheme?
Azurity holds the FDA application for Feraheme (NDA022180, approved June 30, 2009).
Is there a generic or store brand of Feraheme?
Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Feraheme product, 1 of them generic. Ask your pharmacist whether one is right for you.
Has Feraheme been recalled?
No recall linked to Feraheme products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Feraheme is

Each Feraheme product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Ferumoxytol (ferumoxytol non-stoichiometric magnetite) · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
ferumoxytol non-stoichiometric magnetite 510 mg/17 mL
injection (intravenous)
Feraheme 1 product, 1 company DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Ferumoxytol (ferumoxytol non-stoichiometric magnetite) →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Feraheme products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA022180AzurityJune 30, 20091

Companies that list Feraheme

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Feraheme products.

Recalls

No recall linked to Feraheme products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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