Belgium· BE-AMP-SAM485146-00
Obizur 500 U
A susoctocog alfa product containing susoctocog alfa, registered in Belgium by Baxalta Innovations. The same ATC class is registered in 11 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Susoctocog alfa is registered in 11 of 19 countries.
Countries holding a registration under ATC B02BD14 (susoctocog alfa), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 7 of them publish a price we can compare per daily dose
Susoctocog alfa · ATC B02BD14
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Susoctocog Alfa
- Manufacturer
- Baxalta Innovations
- Country
- Belgium (BE)
- ATC code
- B02BD14
- ATC class
- Susoctocog alfa
- Defined daily dose
- 14 TSD, E
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb3667060
- be_apb7721079
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Susoctocog alfa in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaOBIZURBaxalta Innovations GmbH, Vídeň
- SpainOBIZUR 500 U POLVO Y DISOLVENTE PARA SOLUCION INYECTABLEBaxalta Innovations Gmbh
- FinlandObizurBaxalta Innovations GmbH
- FranceOBIZUR 500 U, poudre et solvant pour solution injectableBAXALTA INNOVATIONS (AUTRICHE)
- United KingdomObizur 500unit powder and solvent for solution for injection vialsTakeda UK Ltd
- IrelandOBIZUR 500 U powder and solvent for solution for injectionBaxter Innovations GmbH
- IcelandObizurBaxalta Innovations GmbH
- Japanスソクトコグ アルファ(遺伝子組換え)武田薬品工業
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Obizur
- Liechtenstein · Obizur
- Norway · Obizur
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/aa9847b5-acb9-4f27-81bb-4653ff30c7fb GET /v1/drugs/aa9847b5-acb9-4f27-81bb-4653ff30c7fb?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",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Obizur 500 U",
"name_fr": "Obizur 500 U",
"name_nl": "Obizur 500 U",
"amp_code": "SAM485146-00",
"strengths": [
"500.0000",
"4.4000"
],
"pack_count": 3,
"substances": [
"Susoctocog Alfa",
"Sucrose",
"Polysorbate 80",
"Sodium"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Susoctocog Alfa",
"authorisation_numbers": [
"EU/1/15/1035/001",
"EU/1/15/1035/003",
"EU/1/15/1035/002"
]
}See everything about susoctocog alfa.
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.