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Prescription medicine

Flurpiridaz f 18 Brand names: Flyrcado

Flurpiridaz f 18 (Flyrcado) is a prescription medicine with an FDA approval on record since 2024. No generic is listed in FDA's NDC Directory.

  • No generic listed

Check it at the source: the flurpiridaz f 18 FDA label on DailyMed (effective July 14, 2026, GE Healthcare Inc.); the NDA 215168 record on Drugs@FDA; every flurpiridaz f 18 label on DailyMed.

Highlights of the record

FDA label of July 14, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Used for

From the label: indications and usage

FLYRCADO is indicated for positron emission tomography (PET) myocardial perfusion imaging (MPI) under rest or stress (pharmacologic or exercise) in adult patients with known or suspected coronary artery disease (CAD) to evaluate for myocardial ischemia and infarction.

Forms and strengths

Injection.

On the market

Earliest approval on file
September 27, 2024 Flyrcado, Ge Hlthcare; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
No generic approved
Labelers listed (NDC)
1 of which 0 under generic applications, 1 under brand applications, repackagers included
Last listed patent
May 13, 2042 Flyrcado injection; not a generic launch date

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
1 through July 30, 2026

What is flurpiridaz f 18 used for?

From the label: indications and usage

FLYRCADO is indicated for positron emission tomography (PET) myocardial perfusion imaging (MPI) under rest or stress (pharmacologic or exercise) in adult patients with known or suspected coronary artery disease (CAD) to evaluate for myocardial ischemia and infarction. FLYRCADO is a radioactive diagnostic drug indicated for positron emission tomography (PET) myocardial perfusion imaging (MPI) under rest or stress (pharmacologic or exercise) in adult patients with known or suspected coronary artery disease (CAD) to evaluate for myocardial ischemia and infarction.

FDA pharmacologic class: Radioactive Diagnostic Agent.

Source: FDA drug label (Flyrcado), NDA215168 (Ge Hlthcare), as published by GE Healthcare Inc., effective July 14, 2026 (SPL set 3bb6caf8-ac98-46c7-a9f0-961e66032705), via openFDA; the full label on DailyMed

Is there a generic for flurpiridaz f 18 (Flyrcado)?

No generic flurpiridaz f 18 is approved (Drugs@FDA, October 8, 2026).

The Orange Book lists 7 patents for Flyrcado injection: the compound patent runs to May 26, 2026, and the last listed entry to May 13, 2042. A patent or exclusivity date is not the date a generic goes on sale: court cases and settlements move it either way.

  • 2024 earliest approval on file
  • 2042 last listed patent

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What do FAERS reports show for flurpiridaz f 18?

The FDA Adverse Event Reporting System holds 1 report that list flurpiridaz f 18 among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 0 are coded as a death and 0 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

The most reported reactions

  • No Adverse Event (a use or a product term, not a reaction)1
  • Radioisotope Scan Abnormal1

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Other radioactive diagnostic agents
the pharmacologic class, with prices and generics
Flurpiridaz f 18 side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other