Belgium· BE-AMP-SAM664599-00
Ziihera 300 mg
A zanidatamab product containing zanidatamab, registered in Belgium by Jazz Pharmaceuticals Ireland. The same ATC class is registered in 10 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Zanidatamab is registered in 10 of 19 countries.
Countries holding a registration under ATC L01FD07 (zanidatamab), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 6 of them publish a price we can compare per daily dose
Zanidatamab · ATC L01FD07
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Zanidatamab
- Manufacturer
- Jazz Pharmaceuticals Ireland
- Country
- Belgium (BE)
- ATC code
- L01FD07
- ATC class
- Zanidatamab
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Zanidatamab in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaZIIHERAJazz Pharmaceuticals Ireland Ltd, Dublin
- FinlandZiiheraJazz Pharmaceuticals Ireland Limited
- United KingdomZiihera 300mg powder for concentrate for solution for infusion vialsJazz Pharmaceuticals UK Ltd
- IrelandZiihera 300 mg powder for concentrate for solution for infusionJazz Pharmaceuticals Ireland Limited
- IcelandZiiheraJazz Pharmaceuticals Ireland Limited
- PolandZiiheraJazz Pharmaceuticals Ireland Ltd
- SwedenZiihera 300 mg Pulver till koncentrat till infusionsvätska, lösningJazz Pharmaceuticals Ireland Limited
- United StatesZIIHERAJazz Pharmaceuticals, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Ziihera
- Liechtenstein · Ziihera
- Norway · Ziihera
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/8980b23b-8d1e-49e4-ba66-140e576138ed GET /v1/drugs/8980b23b-8d1e-49e4-ba66-140e576138ed?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 for concentrate for solution for infusion",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Ziihera 300 mg",
"name_fr": "Ziihera 300 mg",
"name_nl": "Ziihera 300 mg",
"amp_code": "SAM664599-00",
"strengths": [
"300.0000",
"300.0000"
],
"pack_count": 2,
"substances": [
"Zanidatamab",
"Disodium Succinate",
"Sucrose",
"Polysorbate 20"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Zanidatamab",
"authorisation_numbers": [
"EU/1/25/1931/001",
"EU/1/25/1931/002"
]
}See everything about zanidatamab.
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.