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MPI INDIUM DTPA IN 111 (INDIUM IN-111 PENTETATE DISODIUM)

GE HEALTHCARE · FDA-approved approved ✓ Verified Jun 2026

MPI INDIUM DTPA IN 111 (generic name: INDIUM IN-111 PENTETATE DISODIUM) is a drug developed by GE HEALTHCARE. It is currently FDA-approved.

MPI INDIUM DTPA IN 111 is a small molecule diagnostic agent. It is used as a synonym for other compounds, including Indium (111 In) Disodium Pentetate.

At a glance

Generic nameINDIUM IN-111 PENTETATE DISODIUM
SponsorGE HEALTHCARE
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

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
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about MPI INDIUM DTPA IN 111

What is MPI INDIUM DTPA IN 111?

MPI INDIUM DTPA IN 111 (INDIUM IN-111 PENTETATE DISODIUM) is a pharmaceutical drug developed by GE HEALTHCARE.

Who makes MPI INDIUM DTPA IN 111?

MPI INDIUM DTPA IN 111 is developed and marketed by GE HEALTHCARE (see full GE HEALTHCARE pipeline at /company/ge-healthcare).

What is the generic name of MPI INDIUM DTPA IN 111?

INDIUM IN-111 PENTETATE DISODIUM is the generic (nonproprietary) name of MPI INDIUM DTPA IN 111.

What development phase is MPI INDIUM DTPA IN 111 in?

MPI INDIUM DTPA IN 111 is FDA-approved (marketed).

What are the side effects of MPI INDIUM DTPA IN 111?

Common side effects of MPI INDIUM DTPA IN 111 include Vomiting, Skin reactions. Serious adverse events: Death, Septic meningitis, Aseptic meningitis, Pyrogenic reactions.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing