Switzerland· 68441001
Scemblix 20 mg, Filmtabletten
A asciminib product containing asciminibum, registered in Switzerland by Novartis Pharma Schweiz AG and dispensed under Swissmedic category A, on the national reimbursement list. The same ATC class is registered in 16 of our 19 countries.
Checked against Swissmedic (Switzerland) on
Informational only — not a medical device.
Where it is registered
Asciminib is registered in 16 of 19 countries.
Countries holding a registration under ATC L01EA06 (asciminib), each read from that country’s own register.
- This record: Switzerland, from Swissmedic (Switzerland)
- 10 of them publish a price we can compare per daily dose
Asciminib · ATC L01EA06
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Spainprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of asciminib costs, country by country.
Normalised to the WHO defined daily dose (80 mg), the median price runs from $0.27 in France to $162.23 in Switzerland — a ×606 gap.
- Switzerland: $162.23 per daily dose (median across products in the class)
- Public list prices, converted to USD at the rate date shown
Asciminib · price per daily dose (80 mg)
USD · FX 28 Sept 2026
- CH Switzerland$162.23
- FR France$0.27
The record
At a glance
Swissmedic (Switzerland)- Active substance
- asciminibum
- Manufacturer
- Novartis Pharma Schweiz AG
- Country
- Switzerland (CH)
- ATC code
- L01EA06
- ATC class
- Asciminib
- Defined daily dose
- 80 mg, O
- Swissmedic category
- A
- Reimbursed
- Yes
- Source register
- Swissmedic (Switzerland)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- gtin7680684410017Blist 60 StkCHF 2022.2
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Asciminib in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaSCEMBLIXNovartis Europharm Limited, Dublin
- SpainSCEMBLIX 20 MG COMPRIMIDOS RECUBIERTOS CON PELICULANovartis Europharm Limited
- FinlandScemblixNovartis Europharm Limited
- FranceSCEMBLIX 20 mg, comprimés pelliculésNOVARTIS EUROPHARM (IRLANDE)
- IrelandScemblix 20 mg film-coated tabletsNovartis Europharm Limited
- IcelandScemblixNovartis Europharm Limited*
- NetherlandsScemblix 20mg, filmomhulde tabletNovartis Europharm Limited
- NorwayScemblixNovartis Europharm Limited
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Scemblix
- Liechtenstein · Scemblix
- Norway · Scemblix
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 Swissmedic (Switzerland). 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/53e4204b-2356-4b37-bc77-a882dcedfa31 GET /v1/drugs/53e4204b-2356-4b37-bc77-a882dcedfa31?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.
{
"unit": null,
"strength": "asciminibum 20 mg",
"valid_from": "2025-06-01",
"limitations": "[{\"description\":\"Asciminib wird vergütet für die Behandlung von erwachsenen Patienten mit Philadelphia-Chromosom-positiver chronisch-myeloischer Leukämie (Ph+ CML) in der chronischen Phase (CP), die neu diagnostiziert wurden oder die zuvor mit einem oder mehr Tyrosinkinaseinhibitoren behandelt wurden und ein Therapieversagen oder eine Unverträglichkeit darauf aufweisen.<br>\\n<br>\\nMit Verschreibung von SCEMBLIX bei neu diagnostizierter Ph+ CML CP berücksichtigt die/der behandelnde Ärztin/Arzt bei der Wahl des passenden Tyrosinkinaseinhibitors umfassend und patientenindividuell den Nutzen und die Kosten. Die Voraussetzungen für eine Vergütung als Erstlinientherapien sind damit ohne weitere Dokumentationspflicht erfüllt. Eine Kostengutsprache ist nicht erforderlich.<br>\\n<br>\\nDie Vergütung erfolgt bis zur Krankheitsprogression. Der Therapieerfolg muss regelmässig gem. den aktuell gültigen Richtlinien unter Berücksichtigung hämatologischer, zytogenetischer (bei Knochenmarkuntersuchungen) oder molekularer Parameter überprüft werden. SCEMBLIX wird bei bestätigter T315I oder V299L Mutation und bei bekanntem Wiederauftreten einer CML-CP nach vorheriger Krankheitsprogression zu AP oder BP nicht vergütet.<br>\\n<br>\\n\",\"costApproval\":null,\"indication\":\"21471.01\",\"isNew\":false,\"limitationCode\":null,\"priceModel\":null,\"validFrom\":\"2025-06-01\",\"validTo\":\"2027-05-31\"}]",
"galenic_form": "Filmtabl 20 mg",
"therapeutic_area": null,
"sl_inclusion_date": "2023-01-01",
"self_retention_pct": 10
}See everything about asciminib.
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.