United States· US:80830-2473_d73504e3-4f96-4751-ae9f-fa6201b28640
Iohexol
A iohexol product containing iohexol, registered in United States by Amneal Pharmaceuticals Private Limited. The same ATC class is registered in 17 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Iohexol is registered in 17 of 19 countries.
Countries holding a registration under ATC V08AB02 (iohexol), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 9 of them publish a price we can compare per daily dose
Iohexol · ATC V08AB02
17 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Sweden
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- IOHEXOL
- Manufacturer
- Amneal Pharmaceuticals Private Limited
- Country
- United States (US)
- ATC code
- V08AB02
- ATC class
- Iohexol
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 1
- ndc1180830-2473-2
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
353 interactions on record for iohexol.
Graded by severity as the source publishes them — 286 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Iohexol · interactions on record
353 records
- 286 severe
- 54 moderate
- 13 info
Most severe, free to view
- MetoclopramideA03FA01severe
- ThiethylperazinA04AB03severe
- TriflupromazinA04AD06severe
- DronabinolA04AD10severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Iohexol in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- Japanイオヘキソール富士製薬工業
- United KingdomIohexol 647mg/ml (Iodine 300mg/ml) solution for injection 100ml bottlesFarmak Pharmaceuticals UK Ltd
- CzechiaOMNIPAQUEGE Healthcare AS, Oslo
- BelgiumOmnipaque 180 mg I/mlGE Healthcare
- SwedenIohexol ICG farma 300 mg I/ml Injektionsvätska, lösningUAB ICG farma
- IrelandOmnipaque 140 mg I/ml Solution for Injection (Glass)GE Healthcare AS
- NetherlandsIohexol ADOH 350 mg I/ml oplossing voor injectieADOH B.V.
- FinlandOmnipaqueGE Healthcare AS
Authorised across Europe · EMA
The same active substance is authorised in 29 EEA countries. Names it is sold under:
- Austria · Accupaque, Iovision
- Belgium · Omnipaque
- Bulgaria · Kopaq, Контамедиа Йох
- Cyprus · Omnipaque
- Czechia · Omnipaque
- Germany · Accupaque, Iovision
- Estonia · Iohexol Imax, Omnipaque
- Spain · Omnipaque
- Finland · Omnipaque
- France · Omnipaque
- United Kingdom (Northern Ireland) · Iohexol Farmak Pharmaceuticals Uk, Iohexol Ge Healthcare
- Greece · Omnipaque
- Croatia · Omnipaque
- Hungary · Iohexol Wogen, Omnipaque
- Ireland · Omnipaque
- Iceland · Omnipaque
- Italy · Omnipaque
- Lithuania · Iohexol Icg Farma, Iohexol Imax
- Luxembourg · Omnipaque
- Latvia · Iohexol Imax, Omnipaque
- Malta · Omnipaque
- Netherlands · Iohexol Adoh, Omnipaque
- Norway · Omnipaque
- Poland · Omnipaque
- Portugal · Iohexol Imax, Omnipaque
- Romania · Omnipaque
- Sweden · Iovision, Omnipaque
- Slovenia · Omnipaque
- Slovakia · Omnipaque
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/4ca462fd-bf23-4b53-8c17-ce49207b9cf1 GET /v1/drugs/4ca462fd-bf23-4b53-8c17-ce49207b9cf1?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "INTRA-ARTICULAR; INTRATHECAL; INTRAVASCULAR; INTRAVENOUS; ORAL; RECTAL",
"source": "ndc",
"strength": "350",
"substance": "IOHEXOL",
"productndc": "80830-2473",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA217737",
"marketing_category": "ANDA"
}See everything about iohexol.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.