Iceland· IS-EU/1/15/1040/008-009
Intuniv
A guanfacine product containing guanfacinum inn hýdróklóríð, registered in Iceland by Takeda Pharmaceuticals International AG Ireland Branch. The same ATC class is registered in 14 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Guanfacine is registered in 14 of 19 countries.
Countries holding a registration under ATC C02AC02 (guanfacine), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 8 of them publish a price we can compare per daily dose
Guanfacine · ATC C02AC02
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Germany
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of guanfacine costs, country by country.
Normalised to the WHO defined daily dose (3 mg), the median price runs from $0.21 in United States to $7.74 in Switzerland — a ×37 gap.
- 2 markets with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
- US figures are pharmacy acquisition cost (CMS NADAC), not retail
Guanfacine · price per daily dose (3 mg)
USD · FX 28 Sept 2026
- CH Switzerland$7.74
- US United States$0.21 (acquisition cost)
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Guanfacinum INN hýdróklóríð
- Manufacturer
- Takeda Pharmaceuticals International AG Ireland Branch
- Country
- Iceland (IS)
- ATC code
- C02AC02
- ATC class
- Guanfacine
- Defined daily dose
- 3 mg, O
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 1
1 priced- ean18585928 stk x1 þpakkiISK 18786
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
163 interactions on record for guanfacine.
Graded by severity as the source publishes them — 30 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
Guanfacine · interactions on record
163 records
- 30 severe
- 133 moderate
Most severe, free to view
- AprepitantA04AD12severe
- DexamethasoneH02AB02severe
- KetoconazoleH02CA03severe
- ChloramphenicolJ01BA01severe
- 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
Guanfacine in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesguanfacineActavis Pharma, Inc.
- United KingdomGuanfacine 4mg modified-release tabletsAccord-UK Ltd
- CanadaAPO-GUANFACINE XRAPOTEX INC
- CzechiaINTUNIVTakeda Pharmaceuticals International AG Ireland Branch, Dublin
- IrelandIntuniv 4 mg prolonged-release tabletsTakeda Pharmaceuticals International AG Ireland Branch
- SpainIntuniv 4mg comprimidos de liberacion prolongadaTakeda Pharmaceuticals International Ag Ireland Branch
- FinlandIntunivTakeda Pharmaceuticals International AG Ireland Branch
- BelgiumIntuniv 4 mgTakeda Pharmaceuticals International Ireland Branch
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Germany · Guanfacin Neuraxpharm
- United Kingdom (Northern Ireland) · Guanfacine Crescent
- Liechtenstein · Intuniv, Paxneury
- Norway · Intuniv, Paxneury
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 Icelandic Medicines Agency (Iceland). 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/671946a8-cd80-42a7-b4e1-e3d05d462e94 GET /v1/drugs/671946a8-cd80-42a7-b4e1-e3d05d462e94?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": "Forðatafla",
"source": "lyfjastofnun",
"atc_raw": "C02AC02",
"marketed": true,
"strength": "4 mg",
"ma_number": "EU/1/15/1040/008-009",
"substance": "Guanfacinum INN hýdróklóríð",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "42264"
}See everything about guanfacine.
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.