Germany· DE-A57-fed960de77b42956
Leustatin
A cladribine product containing cladribine, registered in Germany by Atnahs Pharma Netherlands B.V.. The same ATC class is registered in 12 of our 19 countries.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
Where it is registered
Cladribine is registered in 12 of 19 countries.
Countries holding a registration under ATC L04AA40 (cladribine), each read from that country’s own register.
- This record: Germany, from EMA Article 57 (European Union)
- 8 of them publish a price we can compare per daily dose
Cladribine · ATC L04AA40
12 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Germany
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of cladribine costs, country by country.
Normalised to the WHO defined daily dose (0.34 mg), the median price runs from $0.048 in France to $90.83 in Switzerland — a ×1908 gap.
- 2 markets with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Cladribine · price per daily dose (0.34 mg)
USD · FX 28 Sept 2026
- CH Switzerland$90.83
- FR France$0.048
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Cladribine
- Manufacturer
- Atnahs Pharma Netherlands B.V.
- Country
- Germany (DE)
- ATC code
- L04AA40
- ATC class
- Cladribine
- Defined daily dose
- 0.34 mg, O
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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.
Interactions
409 interactions on record for cladribine.
Graded by severity as the source publishes them — 326 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
Cladribine · interactions on record
409 records
- 326 severe
- 79 moderate
- 4 info
Most severe, free to view
- PrednisoloneA07EA01severe
- HydrocortisoneA07EA02severe
- PrednisoneA07EA03severe
- BetamethasoneA07EA04severe
- 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
Cladribine in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaLEUJECTAtnahs Pharma Netherlands B.V., Amsterdam
- United StatesCladribineHisun Pharmaceuticals USA, Inc.
- FinlandLeujectAtnahs Pharma Netherlands B.V.
- SpainLEUSTATIN 1 MG/ML SOLUCION PARA PERFUSIONAtnahs Pharma Netherlands Bv.
- SwitzerlandLitak 10, Injektions- / InfusionslösungLipomed AG
- NetherlandsLeustatin 2 mg/ml oplossing voor injectieAtnahs Pharma Netherlands B.V.
- PolandBiodribinSieć Badawcza Łukasiewicz – Instytut Chemii Przemysłowej im. Prof. I. Mościckiego
- United KingdomLeustat 10mg/10ml solution for infusion vialsAtnahs Pharma UK Ltd
Authorised across Europe · EMA
The same active substance is authorised in 22 EEA countries. Names it is sold under:
- Austria · Leuject
- Belgium · Leustatin
- Bulgaria · Леуджект
- Czechia · Leuject
- Spain · Leustatin
- Finland · Leuject
- France · Leustatine
- United Kingdom (Northern Ireland) · Cladribine Zentiva, Leustat
- Greece · Leustatin
- Croatia · Leuject
- Hungary · Leuject
- Iceland · Mavenclad
- Italy · Leustatin
- Liechtenstein · Mavenclad
- Luxembourg · Leustatin
- Netherlands · Leustatin
- Norway · Leuject, Mavenclad
- Poland · Biodribin, Leuject
- Portugal · Cladribina Generis, Leustatin
- Romania · Leuject
- Sweden · Leuject
- Slovenia · Leuject
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 EMA Article 57 (European Union). 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/a959ef1a-554f-4ec1-83a3-ed8744d696ec GET /v1/drugs/a959ef1a-554f-4ec1-83a3-ed8744d696ec?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.
{
"pzn": null,
"route": "Subcutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Cladribine",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about cladribine.
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.