Ireland· IE-PA-EU/1/25/2013/001
KYGEVVI 2 g/2 g powder for oral solution
A doxecitine and doxribtimine product containing doxecitine + doxribtimine, registered in Ireland by UCB Pharma S.A.. The same ATC class is registered in 9 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Doxecitine and doxribtimine is registered in 9 of 19 countries.
Countries holding a registration under ATC A16AX29 (doxecitine and doxribtimine), 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
Doxecitine and doxribtimine · ATC A16AX29
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
HPRA (Ireland)- Active substance
- Doxecitine + Doxribtimine
- Manufacturer
- UCB Pharma S.A.
- Country
- Ireland (IE)
- ATC code
- A16AX29
- ATC class
- Doxecitine and doxribtimine
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/25/2013/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Doxecitine and doxribtimine in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaKYGEVVIUCB Pharma SA, Brusel
- FinlandKYGEVVIUCB Pharma SA
- FranceKYGEVVI 2 g/2 g, poudre pour solution buvableUCB PHARMA BELGIQUE
- IcelandKYGEVVIUCB Pharma S.A.*
- NetherlandsKYGEVVI 2 g/2 g poeder voor drankUCB Pharma S.A.
- SwedenKYGEVVI 2 g/2 g Pulver till oral lösningUCB Pharma S.A.
- United StatesKYGEVVIUCB, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Kygevvi
- Liechtenstein · Kygevvi
- Norway · Kygevvi
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 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/db9b810c-1104-4f6a-8b05-b4819c16895c GET /v1/drugs/db9b810c-1104-4f6a-8b05-b4819c16895c?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": "Powder for oral solution",
"routes": [
"Oral use"
],
"source": "hpra",
"atc_all": [
"A16AX29"
],
"strength": null,
"pa_number": "EU/1/25/2013/001",
"substances": [
"Doxecitine",
"Doxribtimine"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "26/03/2026",
"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 doxecitine and doxribtimine.
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.