Czechia· CZ-0290502
ENFLONSIA
A clesrovimab product containing clesrovimab, registered in Czechia by Merck Sharp & Dohme B.V., Haarlem. The same ATC class is registered in 11 of our 19 countries.
Checked against SÚKL (Czech Republic) on
Informational only — not a medical device.
Where it is registered
Clesrovimab is registered in 11 of 19 countries.
Countries holding a registration under ATC J06BD10 (clesrovimab), each read from that country’s own register.
- This record: Czechia, from SÚKL (Czech Republic)
- 9 of them publish a price we can compare per daily dose
Clesrovimab · ATC J06BD10
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Norwayprice
- Polandprice
- Switzerlandprice
- United Statesprice
The record
At a glance
SÚKL (Czech Republic)- Active substance
- CLESROVIMAB
- Manufacturer
- Merck Sharp & Dohme B.V., Haarlem
- Country
- Czechia (CZ)
- ATC code
- J06BD10
- ATC class
- Clesrovimab
- Reimbursed
- Not published by this register
- Source register
- SÚKL (Czech Republic)
- Last checked
- September 28, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Clesrovimab in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainENFLONSIA 105 MG SOLUCION INYECTABLE EN JERINGA PRECARGADAMerck Sharp & Dohme B.V.
- BelgiumEnflonsia 105 mgMerck Sharp & Dohme
- NorwayEnflonsiaMerck Sharp & Dohme B.V.
- PolandEnflonsiaMerck Sharp & Dohme B.V.
- SwedenEnflonsia 105 mg Injektionsvätska, lösning i förfylld sprutaMerck Sharp & Dohme BV
- IcelandEnflonsiaMerck Sharp & Dohme B.V.*
- SwitzerlandEnflonsia
- FinlandEnflonsiaMerck Sharp & Dohme B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Enflonsia
- Liechtenstein · Enflonsia
- Norway · Enflonsia
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 SÚKL (Czech Republic). 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/fda9531b-4734-4344-8197-00a8f9256629 GET /v1/drugs/fda9531b-4734-4344-8197-00a8f9256629?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": "INJ SOL ISP",
"source": "sukl",
"strength": "105MG",
"pack_size": "10X0,7ML+10J",
"substance": "CLESROVIMAB",
"cz_kod_sukl": "0290502",
"product_type": "BT",
"substance_codes": "1398",
"registration_state": "R",
"registration_number": "EU/1/25/1984/005"
}See everything about clesrovimab.
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.