Sweden· SE-20190408000062
Ontruzant 420 mg Pulver till koncentrat till infusionsvätska, lösning
A medicinal product containing trastuzumab, registered in Sweden by Samsung Bioepis NL B.V..
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Trastuzumab
- Manufacturer
- Samsung Bioepis NL B.V.
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer20190408000062
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Trastuzumab in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaDAZUBLYSCuraTeQ Biologics (Malta) Limited, Floriana
- FinlandDazublysCuraTeQ Biologics (Malta) Limited
- BelgiumDazublys 420 mgCuraTeQ Biologics (Malta)
- PolandHerzumaCelltrion Healthcare Hungary Kft.
- IcelandHerzumaCelltrion Healthcare Hungary Kft.
- SpainHERZUMA 420 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONCelltrion Healthcare Hungary Kft.
- IrelandHerzuma 420 mg powder for concentrate for solution for infusionCelltrion Healthcare Hungary Kft.
- United KingdomHerzuma 420mg powder for concentrate for solution for infusion vialsCelltrion Healthcare UK Ltd
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Dazublys, Herceptin
- Liechtenstein · Dazublys, Herceptin
- Norway · Dazublys, Herceptin
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 Swedish Medical Products Agency (Sweden). 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/ad11323a-3db4-4849-b603-3b95a1f17974 GET /v1/drugs/ad11323a-3db4-4849-b603-3b95a1f17974?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.
{
"source": "lakemedelsverket",
"doc_types": [
"EMA",
"EPAR"
],
"se_npl_id": "20190408000062",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20190408000062",
"product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/ontruzant"
}See everything about trastuzumab.
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.