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fudr

Pharmaranks rates Fudr 2.9/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Fudr (Floxuridine) is an antimetabolite used to treat Stomach Neoplasms, Colorectal Neoplasms.

Floxuridine · by Hospira

58/100Limited · 1 source

Based on 1 source · Recall-safety score from FDA recall history — this product's own recalls and its manufacturer's record. Not an efficacy or quality rating. methodology →

Rated against independent regulatory sources·Last updated October 7, 2026·How we rate
Verified againstopenFDANIH DailyMedRxClass

Key facts

Active ingredient
Floxuridine
Drug class
Antimetabolite
Form
Injectable
Strength
Floxuridine 500MG/VIAL **Federal Register Determination That Product was not Discontinued or Withdrawn for Safety or Effectiveness reasons**
Type
Prescription (Rx)
Brand or generic
Brand-name
Manufacturer
Hospira
FDA application
NDA016929
Availability
Discontinued (per FDA)

Drug class

May treat (source: NIH RxClass)

Dosage forms

Injectable

The forms currently marketed in the U.S., per the FDA National Drug Code Directory.

Ways to save

Ask for the generic

Same active ingredient, far cheaper. Is there a generic? →

Request a 90-day supply

Bulk fills usually lower the per-dose price vs monthly refills.

Use copay cards

Manufacturer copay cards & patient-assistance programs — especially for brand drugs.

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Frequently asked questions

What does Fudr treat?
Fudr (Floxuridine) may be used to treat stomach neoplasms, colorectal neoplasms, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.
How is Fudr rated?
pharmaranks gives Fudr a composite score of 2.9 out of 5, currently based on 1 weighted source (FDA regulatory recall-safety data weighted highest). See our methodology at /how-we-rate.
Is there a coupon or discount for Fudr?
pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Fudr. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
Who makes Fudr?
Fudr is marketed by Hospira. You can see Hospira's full profile, rating, and other products on pharmaranks.
Is Fudr a brand-name or generic drug?
Fudr is a brand-name product with the active ingredient Floxuridine.
Is Fudr available over the counter?
No. Fudr is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
What forms does Fudr come in?
Fudr is currently marketed as injectable, per the FDA's National Drug Code Directory.
What class of drug is Fudr?
Fudr is classified as antimetabolite, per the FDA's Established Pharmacologic Class.
Is Fudr FDA-registered?
Fudr is on record with the U.S. FDA under application number NDA016929. You can verify this on its official FDA label.
Has Fudr been recalled by the FDA?
Fudr has no FDA recalls recorded under its own application in the openFDA enforcement database. Its recall-safety score reflects its manufacturer's overall recall record. This is general reference, not medical advice — check the FDA recall database for the latest alerts.
Is Fudr safe?
There's no single safe-or-not verdict. pharmaranks gives Fudr a recall-safety score of 58/100, based on its FDA recall history (no recalls under its own FDA application) — not an efficacy or side-effect rating. Review its FDA-label side effects and warnings before use, and always consult a licensed professional.

Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.

What people report to the FDA about FLOXURIDINE

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 168 reports naming FLOXURIDINE — the active ingredient in Fudr, and the FDA flagged 90% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • diarrhoea18 reports
  • hepatic steatosis13 reports
  • steatohepatitis12 reports
  • alanine aminotransferase increased10 reports
  • nausea9 reports
  • tachycardia9 reports
  • abdominal pain8 reports
  • neutropenia8 reports

Read these as a signal, not a rate. A report does not mean FLOXURIDINE caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.

Source: openFDA drug/event (FAERS), retrieved September 25, 2026.

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