Belgium· BE-AMP-SAM593644-00
Aspaveli 1080 mg
A pegcetacoplan product containing pegcetacoplan, registered in Belgium by Swedish Orphan Biovitrum (Publ). The same ATC class is registered in 12 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Pegcetacoplan is registered in 12 of 19 countries.
Countries holding a registration under ATC L04AJ03 (pegcetacoplan), 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
Pegcetacoplan · ATC L04AJ03
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Pegcetacoplan
- Manufacturer
- Swedish Orphan Biovitrum (Publ)
- Country
- Belgium (BE)
- ATC code
- L04AJ03
- ATC class
- Pegcetacoplan
- Defined daily dose
- 0.3 g, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 3
- be_apb4683108
- be_apb7737497
- be_apb4683090
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pegcetacoplan in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaASPAVELISwedish Orphan Biovitrum AB (publ), Stockholm
- SpainASPAVELI 1080 MG SOLUCION PARA PERFUSIONSwedish Orphan Biovitrum Ab (Publ)
- IcelandASPAVELI*Swedish Orphan Biovitrum AB (publ)
- NorwayAspaveliApellis Ireland Limited
- SwedenASPAVELI 1080 mg Infusionsvätska, lösningSwedish Orphan Biovitrum AB (publ)
- United StatesEmpaveliApellis Pharmaceuticals, Inc.
- SwitzerlandAspaveli
- FranceASPAVELI 1080 mg, solution pour perfusionSWEDISH ORPHAN BIOVITRUM (SUEDE)
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Aspaveli
- Liechtenstein · Aspaveli
- Norway · Aspaveli
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/5c61319a-06e8-461f-8bd5-7b024c202bb6 GET /v1/drugs/5c61319a-06e8-461f-8bd5-7b024c202bb6?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 infusion",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Aspaveli 1080 mg",
"name_fr": "Aspaveli 1080 mg",
"name_nl": "Aspaveli 1080 mg",
"amp_code": "SAM593644-00",
"strengths": [
"54.0000",
"41.0000"
],
"pack_count": 2,
"substances": [
"Pegcetacoplan",
"Sodium Acetate Trihydrate",
"Sodium Hydroxide",
"Sorbitol"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Pegcetacoplan",
"authorisation_numbers": [
"EU/1/21/1595/001",
"EU/1/21/1595/002"
]
}See everything about pegcetacoplan.
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.