Belgium· BE-AMP-SAM554257-00
Beovu 120 mg/ml
A brolucizumab product containing brolucizumab, registered in Belgium by Novartis Europharm. The same ATC class is registered in 13 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Brolucizumab is registered in 13 of 19 countries.
Countries holding a registration under ATC S01LA06 (brolucizumab), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 8 of them publish a price we can compare per daily dose
Brolucizumab · ATC S01LA06
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Brolucizumab
- Manufacturer
- Novartis Europharm
- Country
- Belgium (BE)
- ATC code
- S01LA06
- ATC class
- Brolucizumab
- Defined daily dose
- 0.0357 DE, IVT
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb4175592
- be_apb7738677
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Brolucizumab in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaBEOVUNovartis Europharm Limited, Dublin
- IcelandBeovuNovartis Europharm Limited*
- SwedenBeovu 120 mg/ml Injektionsvätska, lösningNovartis Europharm Limited
- FranceBEOVU 120 mg/ml, solution injectable en seringue préremplieNOVARTIS EUROPHARM (IRLANDE)
- NetherlandsBeovu 120 mg/ml, oplossing voor injectieNovartis Europharm Limited
- PolandBeovuNovartis Europharm Limited
- IrelandBeovu 120 mg/ml solution for injection in pre-filled syringeNovartis Europharm Limited
- SwitzerlandBeovu
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Beovu
- Liechtenstein · Beovu
- Norway · Beovu
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/6278a5ae-8b90-4dc3-9cee-4a9b6c43fe39 GET /v1/drugs/6278a5ae-8b90-4dc3-9cee-4a9b6c43fe39?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": "Solution for injection in pre-filled syringe",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Beovu 120 mg/ml",
"name_fr": "Beovu 120 mg/ml",
"name_nl": "Beovu 120 mg/ml",
"amp_code": "SAM554257-00",
"strengths": [
"120.0000"
],
"pack_count": 1,
"substances": [
"Brolucizumab",
"Sucrose",
"Polysorbate 80"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Brolucizumab",
"authorisation_numbers": [
"EU/1/19/1417/001"
]
}See everything about brolucizumab.
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.