Last reviewed · How we verify

MANGAFODIPIR

FDA-approved approved Small molecule Quality 30/100

MANGAFODIPIR is a paramagnetic contrast agent, a small molecule modality developed for use in magnetic resonance imaging (MRI). It was originally developed and is currently owned by a pharmaceutical company. MANGAFODIPIR is approved by the FDA for the indication of liver imaging, with an approval date of 1997. The drug is off-patent, meaning it is no longer protected by patents, and there are no generic manufacturers. As an off-patent drug, its commercial status is uncertain.

At a glance

Generic nameMANGAFODIPIR
Drug classParamagnetic Contrast Agent
ModalitySmall molecule
Therapeutic areaGastroenterology
PhaseFDA-approved
First approval1997

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: