Belgium· BE-AMP-SAM527733-00

Fasenra 30 mg

A benralizumab product containing benralizumab, registered in Belgium by AstraZeneca. The same ATC class is registered in 16 of our 19 countries.

ATC R03DX10

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedFasenra 30 mgATCR03DX10REGISTER NO.BE-AMP-SAM527733-00PACKS LISTED4CHECKEDSeptember 26, 2026

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: Belgium, from FAMHP / AFMPS (Belgium)
  • 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
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

FAMHP / AFMPS (Belgium)
Active substance
Benralizumab
Manufacturer
AstraZeneca
Country
Belgium (BE)
ATC code
R03DX10
ATC class
Benralizumab
Defined daily dose
0.54 mg, P
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 4

2 priced
  • be_apb
    3678448
    EUR 2422.49
  • be_apb
    4169637
    EUR 2422.49
  • be_apb
    7727993
  • be_apb
    7723125

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.

All benralizumab products

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 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/89235ca7-129b-4af6-879d-33874a4e528d
GET /v1/drugs/89235ca7-129b-4af6-879d-33874a4e528d?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": "Fasenra 30 mg",
  "name_fr": "Fasenra 30 mg",
  "name_nl": "Fasenra 30 mg",
  "amp_code": "SAM527733-00",
  "strengths": [
    "30.0000"
  ],
  "pack_count": 4,
  "substances": [
    "Benralizumab",
    "Polysorbate 20"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Benralizumab",
  "authorisation_numbers": [
    "EU/1/17/1252/001"
  ]
}

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.