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Molecule

Iohexol

Radiographic Contrast Agent
Available on requestContrast media and diagnostics
Presentations
28
Brands
1
Manufacturers
1
Available from stock
0

Iohexol is a radiographic contrast agent indicated for intrathecal, intra-arterial, intravenous, oral, rectal, intraarticular, and body cavity imaging procedures in adults and pediatric patients, among other approved uses. MedsAcross supplies Iohexol for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Radiographic Contrast Agent, X-Ray Contrast Activity
ATC classification
V08AB02 Iohexol · Iodinated contrast, subgroup V08AB
US FDA first approval
26 December 1985
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous, Oral, Intravascular, Intra-articular, Intrathecal, Rectal
Dosage forms
Injection, Oral solution
Identifiers
UNII 4419T9MX03RxCUI 5956CAS 66108-95-0DrugBank DB01362Q410683

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

OMNIPAQUE is a radiographic contrast agent indicated for intrathecal, intra-arterial, intravenous, oral, rectal, intraarticular, and body cavity imaging procedures in adults and pediatric patients.

Source: US FDA prescribing information

How it works

The iodine atoms in iohexol provide attenuation of X-rays in direct proportion to the concentration of iohexol. Since concentration changes over time, iohexol provides time-dependent image contrast which may assist in visualizing body structures.

Source: US FDA prescribing information

Dosing overview

For each imaging procedure, specific dosage forms, concentrations, and presentations are recommended. Individualize the concentration and volume according to the specific dosing tables and accounting for factors such as age, body weight, and condition of the patient, and the equipment and imaging technique used. See full prescribing information for complete dosing and administration information.

Source: US FDA prescribing information

Contraindications

OMNIPAQUE for hysterosalpingography is contraindicated during pregnancy or suspected pregnancy, menstruation or when menstruation is imminent, within 6 months after termination of pregnancy, within 30 days after conization or curettage, when signs of infection are present in any portion of the genital tract including the external genitalia, and when reproductive tract neoplasia is known or suspected because of the risk of peritoneal spread of neoplasm.

Source: US FDA prescribing information

Warnings and precautions

Boxed warning (risks associated with intrathecal administration of omnipaque injection 140): mg IODINE/mL and 350 mg IODINE/mL Use only the OMNIPAQUE iodine concentrations and presentations recommended for intrathecal procedure. Hypersensitivity Reactions: Life-threatening or fatal reactions can occur. Always have emergency equipment and trained personnel available. Acute Kidney Injury: Acute injury including renal failure can occur. Minimize dose and maintain adequate hydration to minimize risk. Cardiovascular Adverse Reactions: Hemodynamic disturbances including shock and cardiac arrest may occur during or after administration. Thyroid Dysfunction in Pediatric Patients 0 to 3 Years of Age: Individualize thyroid function monitoring based on risk factors such as prematurity.

Source: US FDA prescribing information

Side effects

The following clinically significant adverse reactions are described elsewhere in the labeling: Risks Associated with Intrathecal Administration of OMNIPAQUE Injection 140 mg Iodine/mL and 350 mg Iodine/mL Risks Associated with Parenteral Administration of OMNIPAQUE Oral Solution Hypersensitivity Reactions Acute Kidney Injury Cardiovascular Adverse Reactions Thromboembolic Events Thyroid Dysfunction in Pediatric Patients 0 to 3 Years of Age Severe Cutaneous Adverse Reactions Most common adverse reactions (incidence ≥ 1%) in adult patients Intrathecal: Headaches, pain including backache, neckache, stiffness and neuralgia, nausea, vomiting, dizziness Intra-arterial or intravenous: Pain, vision abnormalities (including blurred vision and photomas), headache, taste perversion, arrhythmias including premature ventricular contractions (PVCs) and premature atrial contractions (PACs)…

Source: US FDA prescribing information

Interactions

Drug-Drug Interactions Metformin In patients with renal impairment, metformin can cause lactic acidosis. Iodinated contrast agents appear to increase the risk of metformin-induced lactic acidosis, possibly as a result of worsening renal function. Stop metformin at the time of, or prior to, OMNIPAQUE administration in patients with an eGFR between 30 and 60 mL/min/1.73 m 2, in patients with a history of hepatic impairment, alcoholism or heart failure, or in patients who will be administered intra-arterial iodinated contrast. Re-evaluate eGFR 48 hours after the imaging procedure, and reinstitute metformin only after renal function is stable. Radioactive Iodine OMNIPAQUE may interfere with thyroid uptake of radioactive iodine (I-131 and I-123) and decrease therapeutic and diagnostic efficacy. Avoid thyroid therapy or testing for up to 6 weeks post OMNIPAQUE.

Source: US FDA prescribing information

Storage

Store at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F). May be stored in a contrast media warmer for up to one month, not to exceed 37°C (98.6°F). OMNIPAQUE Oral Solution: Store between 0°C and 30°C (32°F to 86°F). Do not freeze. Discard any product that is inadvertently frozen, as freezing may compromise the closure integrity of the immediate container. Protect from light.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

28 presentations of Iohexol, sorted by availability.

MedicineManufacturerRegisterAvailability
Omnipaque 12000 mg/50 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 9000 mg/30 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Iohexol 15000 mg/50 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGeneric name—US FDAAvailable on request
Iohexol 17500 mg/50 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGeneric name—US FDAAvailable on request
Iohexol 22500 mg/75 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGeneric name—US FDAAvailable on request
Iohexol 26250 mg/75 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGeneric name—US FDAAvailable on request
Iohexol 30000 mg/100 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGeneric name—US FDAAvailable on request
Iohexol 35000 mg/100 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGeneric name—US FDAAvailable on request
Omnipaque 12 mg/mL oral solutionOralGE HealthcareUS FDAAvailable on request
Omnipaque 15000 mg/50 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 150000 mg/500 mL injectionIntravenousGE HealthcareUS FDAAvailable on request
Omnipaque 17500 mg/50 mL injectionIntra-articular, intravascular, intravenous, oralGE HealthcareUS FDAAvailable on request
Omnipaque 175000 mg/500 mL injectionIntravenousGE HealthcareUS FDAAvailable on request
Omnipaque 1800 mg/10 mL injectionIntrathecal, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 2400 mg/10 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 24000 mg/100 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 26250 mg/75 mL injectionIntra-articular, intravascular, intravenous, oralGE HealthcareUS FDAAvailable on request
Omnipaque 3000 mg/10 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 30000 mg/100 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 35000 mg/100 mL injectionIntra-articular, intravascular, intravenous, oralGE HealthcareUS FDAAvailable on request
Omnipaque 37500 mg/125 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 43750 mg/125 mL injectionIntra-articular, intravascular, intravenous, oralGE HealthcareUS FDAAvailable on request
Omnipaque 45000 mg/150 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 4800 mg/20 mL injectionIntra-articular, intrathecal, intravascular, intravenous, oral, rectalGE HealthcareUS FDAAvailable on request
Omnipaque 52500 mg/150 mL injectionIntra-articular, intravascular, intravenous, oralGE HealthcareUS FDAAvailable on request
Omnipaque 7000 mg/50 mL injectionIntravascular, intravenousGE HealthcareUS FDAAvailable on request
Omnipaque 70000 mg/200 mL injectionIntra-articular, intravascular, intravenous, oralGE HealthcareUS FDAAvailable on request
Omnipaque 9 mg/mL oral solutionOralGE HealthcareUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 26 December 1985Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Iohexol available for export from India?

Yes, on request. MedsAcross lists 28 presentations of Iohexol and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Iohexol have?

The catalogue lists 1 brand names for Iohexol, including Omnipaque.

Is Iohexol approved by the US FDA?

Yes. The US FDA first approved Iohexol on 26 December 1985, according to Drugs@FDA.

Does Iohexol need cold chain shipping?

No listed presentation of Iohexol is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Iohexol in?

Iohexol is classified under ATC code V08AB02 (Iohexol).

References

  1. OMNIPAQUE prescribing information (GE Healthcare). U.S. National Library of Medicine, DailyMed. Retrieved 7 April 2026

Request Iohexol for export supply

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