Belgium· BE-AMP-SAM253547-00
Simulect 10 mg
A basiliximab product containing basiliximab, registered in Belgium by Novartis Europharm. The same ATC class is registered in 14 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
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: Belgium, from FAMHP / AFMPS (Belgium)
- 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
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Basiliximab
- Manufacturer
- Novartis Europharm
- Country
- Belgium (BE)
- ATC code
- L04AC02
- ATC class
- Basiliximab
- Defined daily dose
- 40 mg, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 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.
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.
- IcelandSimulectNovartis Europharm Limited*
- FinlandSimulectNovartis Europharm Limited
- SwedenSimulect 10 mg Pulver och vätska till injektions-/infusionsvätska, lösningNovartis Europharm Limited
- PolandSimulectNovartis Europharm Limited
- IrelandSimulect 10 mg powder and solvent for solution for injection or infusionNovartis Europharm Limited
- CzechiaSIMULECTNovartis Europharm Limited, Dublin
- United KingdomSimulect 10mg powder and solvent for solution for injection vialsNovartis Pharmaceuticals UK Ltd
- NorwaySimulectNovartis Europharm Limited (1)
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 FAMHP / AFMPS (Belgium). 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/279dd1d2-ccbe-4c8a-9ef3-271dec8249fa GET /v1/drugs/279dd1d2-ccbe-4c8a-9ef3-271dec8249fa?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": "Powder and solvent for solution for injection/infusion",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Simulect 10 mg",
"name_fr": "Simulect 10 mg",
"name_nl": "Simulect 10 mg",
"amp_code": "SAM253547-00",
"strengths": [
"10.0000"
],
"pack_count": 1,
"substances": [
"Basiliximab",
"Disodium Hydrogen Phosphate",
"Mannitol",
"Potassium Dihydrogen Phosphate",
"Sodium Chloride",
"Sucrose"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Basiliximab",
"authorisation_numbers": [
"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.