Iceland· IS-IS/1/21/128/01
Sufentanil hameln
A sufentanil product containing sufentanilum inn cítrat, registered in Iceland by hameln pharma gmbh. The same ATC class is registered in 11 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Sufentanil is registered in 11 of 19 countries.
Countries holding a registration under ATC N01AH03 (sufentanil), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 7 of them publish a price we can compare per daily dose
Sufentanil · ATC N01AH03
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Sufentanilum INN cítrat
- Manufacturer
- hameln pharma gmbh
- Country
- Iceland (IS)
- ATC code
- N01AH03
- ATC class
- Sufentanil
- Defined daily dose
- 30 mcg, P
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 2
2 priced- ean9823992 ml x10 lykjurISK 6449
- ean9895772 ml x5 lykjurISK 5555
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
216 interactions on record for sufentanil.
Graded by severity as the source publishes them — 20 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
Sufentanil · interactions on record
216 records
- 20 severe
- 158 moderate
- 38 info
Most severe, free to view
- OndansetronA04AA01severe
- GranisetronA04AA02severe
- DolasetronA04AA04severe
- PalonosetronA04AA05severe
- 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
Sufentanil in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaDZUVEOLaboratoire Aguettant, Lyon
- BelgiumDzuveo 30 µgLaboratoire Aguettant
- FinlandDzuveoLaboratoire Aguettant
- GermanySufentaPiramal Critical Care B.V.
- FranceDZUVEO 30 microgrammes, comprimé sublingualAGUETTANT
- SwitzerlandSufenta forte, InjektionslösungPiramal Critical Care Limited, London, Zweigniederlassung Rüschlikon
- PolandDzuveoLaboratoire Aguettant
- NetherlandsDzuveo 30 microgram tabletten voor sublinguaal gebruikLaboratoire Aguettant
Authorised across Europe · EMA
The same active substance is authorised in 25 EEA countries. Names it is sold under:
- Austria · Sufenta, Sufentanil Hameln
- Belgium · Sufenta, Sufenta Forte
- Cyprus · Sofentil
- Czechia · Sontilen, Sufenta
- Germany · Sufenta, Sufenta Epidural
- Denmark · Sofentil, Sufenta
- Spain · Safentil, Secufen
- Finland · Sufenta, Sufenta Forte
- France · Sufenta, Sufentanil Renaudin
- United Kingdom (Northern Ireland) · Dzuveo
- Croatia · Sofentil, Sufentanil Altamedics
- Hungary · Sufentanil Hameln, Sufentanil Torrex
- Italy · Disufen, Sufentanil Hameln
- Liechtenstein · Dzuveo, Sufenta
- Luxembourg · Sufenta, Sufenta Forte
- Latvia · Sontilen
- Malta · Sofentil
- Netherlands · Narcomed, Sufenta
- Norway · Dzuveo, Sufenta
- Poland · Sufentanil Chiesi, Sufentanil Hameln
- Portugal · Sontilen, Sufenta
- Romania · Sofentil
- Sweden · Sufenta, Sufentanil Hameln
- Slovenia · Sufentanil Hameln
- Slovakia · Sofentil, Sufentanil Chiesi
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/57b73909-e5ea-447e-9f4a-02b49b15fc75 GET /v1/drugs/57b73909-e5ea-447e-9f4a-02b49b15fc75?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": "Stungulyf/innrennslislyf, lausn",
"source": "lyfjastofnun",
"atc_raw": "N01AH03",
"marketed": false,
"strength": "5 míkróg/ml",
"ma_number": "IS/1/21/128/01",
"substance": "Sufentanilum INN cítrat",
"other_info": null,
"legal_status": "(R X) Eftirritunarskylt (og lyfseðilsskylt)\r\n(H) Sjúkrahúsmerkt",
"ma_issued_serial": "44551"
}See everything about sufentanil.
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.