Czechia· CZ-0027628

SIMULECT

A basiliximab product containing basiliximab, registered in Czechia by Novartis Europharm Limited, Dublin. The same ATC class is registered in 14 of our 19 countries.

ATC L04AC02

Checked against SÚKL (Czech Republic) on

Informational only — not a medical device.

SOURCE REGISTER · CZSÚKL (Czech Republic)normalisedSIMULECTATCL04AC02REGISTER NO.CZ-0027628PACKS LISTED0CHECKEDSeptember 28, 2026

Where it is registered

Basiliximab is registered in 14 of 19 countries.

Countries holding a registration under ATC L04AC02 (basiliximab), 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

Basiliximab · ATC L04AC02

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

SÚKL (Czech Republic)
Active substance
BASILIXIMAB
Manufacturer
Novartis Europharm Limited, Dublin
Country
Czechia (CZ)
ATC code
L04AC02
ATC class
Basiliximab
Defined daily dose
40 mg, P
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.

Interactions

60 interactions on record for basiliximab.

Graded by severity as the source publishes them — 27 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

Basiliximab · interactions on record

60 records

  • 27 severe
  • 26 moderate
  • 7 minor

Most severe, free to view

  • CladribineL01BB04severe
  • Talimogene laherparepvecL01XL02severe
  • Talimogen laherparepvecL01XX51severe
  • LeflunomidL04AA13severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Basiliximab in 14 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All basiliximab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Simulect
  • Liechtenstein · Simulect
  • Norway · Simulect

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/c67a7d2f-a2ee-4de8-9ddf-59887616177b
GET /v1/drugs/c67a7d2f-a2ee-4de8-9ddf-59887616177b?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/INF PSO LQF",
  "source": "sukl",
  "strength": "10MG",
  "pack_size": "1+1X5ML AMP",
  "substance": "BASILIXIMAB",
  "cz_kod_sukl": "0027628",
  "product_type": "BT",
  "substance_codes": "15365",
  "registration_state": "R",
  "registration_number": "EU/1/98/084/002"
}

See everything about basiliximab.

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.