Poland· PL-100200010
Sufentanil Chiesi
A sufentanil product containing sufentanilum, registered in Poland by Chiesi Pharmaceuticals GmbH. The same ATC class is registered in 11 of our 19 countries.
Checked against URPL (Poland) 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: Poland, from URPL (Poland)
- 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
URPL (Poland)- Active substance
- Sufentanilum
- Manufacturer
- Chiesi Pharmaceuticals GmbH
- Country
- Poland (PL)
- ATC code
- N01AH03
- ATC class
- Sufentanil
- Defined daily dose
- 30 mcg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05909991024611
- gtin05909991024628
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
- NetherlandsDzuveo 30 microgram tabletten voor sublinguaal gebruikLaboratoire Aguettant
- SpainDZUVEO 30 MICROGRAMOS COMPRIMIDO SUBLINGUALLaboratoire 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
- Iceland · Dzuveo, Sufenta
- Italy · Disufen, Sufentanil Hameln
- Liechtenstein · Dzuveo, Sufenta
- Luxembourg · Sufenta, Sufenta Forte
- Latvia · Sontilen
- Malta · Sofentil
- Netherlands · Narcomed, Sufenta
- Norway · Dzuveo, Sufenta
- 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 URPL (Poland). 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/4e807e8d-888f-4ea9-bd21-a435f12dd4a2 GET /v1/drugs/4e807e8d-888f-4ea9-bd21-a435f12dd4a2?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": "Roztwór do wstrzykiwań",
"source": "urpl",
"strength": "50 mcg/ml, (250 mcg/5 ml, 1 mg/20 ml)",
"packaging": "05909991024611 ¦ Lz ¦ 22284\n5 amp. 5 ml\n05909991024628 ¦ Lz ¦ 22285\n5 amp. 20 ml",
"substance": "Sufentanili citras 0,375 mg/5 ml + Sufentanili citras 1,5 mg/20 ml",
"common_name": "Sufentanilum",
"pl_product_id": "100200010",
"pozwolenie_nr": "10246",
"auth_procedure": "NAR",
"authorisation_validity": "Bezterminowe"
}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.