Netherlands· NL-0ff7fd55688a
Fasenra 30 mg oplossing voor injectie in voorgevulde spuit
A benralizumab product containing benralizumab, registered in Netherlands by AstraZeneca AB. The same ATC class is registered in 16 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Benralizumab is registered in 16 of 19 countries.
Countries holding a registration under ATC R03DX10 (benralizumab), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 10 of them publish a price we can compare per daily dose
Benralizumab · ATC R03DX10
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- BENRALIZUMAB
- Manufacturer
- AstraZeneca AB
- Country
- Netherlands (NL)
- ATC code
- R03DX10
- ATC class
- Benralizumab
- Defined daily dose
- 0.54 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/17/1252
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Benralizumab in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceFASENRA 30 mg, solution injectable en seringue préremplieASTRAZENECA AB
- IrelandFasenra 30 mg solution for injectionAstraZeneca AB
- FinlandFasenraOrifarm Oy
- United StatesFASENRAAstraZeneca Pharmaceuticals LP
- Japanベンラリズマブ(遺伝子組換え)アストラゼネカ
- NorwayFasenraAstraZeneca AB (2)
- SpainFASENRA 30 MG SOLUCION INYECTABLE EN JERINGA PRECARGADAAstrazeneca Ab
- United KingdomFasenra 30mg/1ml solution for injection pre-filled pensAstraZeneca UK Ltd
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Fasenra
- Liechtenstein · Fasenra
- Norway · Fasenra
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 CBG-MEB (Netherlands). 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/dd3ad8dc-c7a2-4cbc-b873-cd7195972ddc GET /v1/drugs/dd3ad8dc-c7a2-4cbc-b873-cd7195972ddc?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": "Oplossing voor injectie",
"route": "Subcutaan gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/fasenra-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Benralizumab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp120336",
"excipients": [
"HISTIDINE, (L-)",
"HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
"POLYSORBAAT 20 (E 432)",
"TREHALOSE (Alpha, Alpha-) 2-WATER",
"WATER VOOR INJECTIE"
],
"substances": [
"BENRALIZUMAB"
],
"leaflet_url": null,
"authorised_at": "2018/01/08",
"procedure_number": "EMEA/H/C/004433",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/17/1252",
"additional_monitoring": "N"
}See everything about benralizumab.
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.