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Ultravist 370 (IOPROMIDE)

Bayer · FDA-approved approved Small molecule

Ultravist 370 works by accumulating in body fluids and tissues, allowing for enhanced contrast in medical imaging.

Ultravist 370 (Iopromide) is a radiographic contrast agent, a small molecule developed by Bayer Healthcare, which remains under the company's ownership. It is used to enhance the visibility of internal structures during medical imaging procedures. Although its target is unknown, it has been FDA-approved since 1995 for various indications. As an off-patent product, there are currently no generic manufacturers. Key safety considerations include its 2.6-hour half-life.

At a glance

Generic nameIOPROMIDE
SponsorBayer
Drug classRadiographic Contrast Agent
ModalitySmall molecule
Therapeutic areaOther
PhaseFDA-approved
First approval1995

Mechanism of action

ULTRAVIST injection is nonionic, water soluble, tri-iodinated x-ray contrast agent for intravascular administration. Intravascular injection of ULTRAVIST injection opacifies those vessels in the path of flow of the contrast agent, permitting radiographic visualization of the internal structures until significant hemodilution occurs.

Approved indications

No approved indications tracked.

Boxed warnings

Common side effects

Key clinical trials

Primary sources

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