Ireland· IE-PA-PA0690/020/001
Technescan MIBI 1mg kit for radiopharmaceutical preparation
A technetium (99mtc) sestamibi product containing tetrakis (2-methylopropyl-isocyanide) copper (i) tetrafluoroborate, registered in Ireland by Curium Netherlands B.V.. The same ATC class is registered in 11 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Technetium (99mtc) sestamibi is registered in 11 of 19 countries.
Countries holding a registration under ATC V09GA01 (technetium (99mtc) sestamibi), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 6 of them publish a price we can compare per daily dose
Technetium (99mtc) sestamibi · ATC V09GA01
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Germany
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
HPRA (Ireland)- Active substance
- Tetrakis (2-methylopropyl-isocyanide) copper (i) tetrafluoroborate
- Manufacturer
- Curium Netherlands B.V.
- Country
- Ireland (IE)
- ATC code
- V09GA01
- ATC class
- Technetium (99mTc) sestamibi
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA0690/020/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under V09GA01
Technetium (99mtc) sestamibi, as other registers publish it.
- CzechiaCARDIO-SPECTMedi-Radiopharma Kft., Érd
- CzechiaCARDIO-SPECTMedi-Radiopharma Kft., Érd
- CzechiaCARDIO-SPECTMedi-Radiopharma Kft., Érd
- CzechiaCARDIO-SPECTMedi-Radiopharma Kft., Érd
- BelgiumCardioliteLantheus Medical Imaging
- FinlandCardioliteLantheus MI UK Limited
- CanadaDRAXIMAGE SESTAMIBIJUBILANT DRAXIMAGE INC. DBA JUBILANT RADIOPHARMA
- BelgiumDraxmibi 1 mgDraximage
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of HPRA (Ireland). 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/abdd38b3-b812-40a0-a683-e34b28f6a74a GET /v1/drugs/abdd38b3-b812-40a0-a683-e34b28f6a74a?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.
{
"form": "Kit for radiopharmaceutical preparation",
"routes": [
"Intravenous use"
],
"source": "hpra",
"atc_all": [
"V09GA01"
],
"strength": null,
"pa_number": "PA0690/020/001",
"substances": [
"Tetrakis (2-methylopropyl-isocyanide) copper (i) tetrafluoroborate"
],
"legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
"market_info": "Marketed",
"authorised_at": "21/11/2008",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about technetium (99mtc) sestamibi.
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.