Sweden· SE-20160427000077
Ocrevus 300 mg Koncentrat till infusionsvätska, lösning
A medicinal product containing ocrelizumab, registered in Sweden by Roche Registration GmbH.
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
- Ocrelizumab
- Manufacturer
- Roche Registration GmbH
- 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_varunummer20160427000077
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ocrelizumab in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandOcrevusParanova Oy
- CzechiaOCREVUSRoche Registration GmbH, Grenzach-Wyhlen
- BelgiumOcrevus 300 mgRoche Registration
- IrelandOcrevus 300 mg concentrate for solution for infusionRoche Registration GmbH
- IcelandOcrevusRoche Registration GmbH*
- NetherlandsOcrevus 300 mg concentraat voor oplossing voor infusieRoche Registration GmbH
- United KingdomOcrevus 300mg/10ml concentrate for solution for infusion vialsRoche Products Ltd
- FranceOCREVUS 300 mg, solution à diluer pour perfusionROCHE REGISTRATION (ALLEMAGNE)
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Ocrevus
- Liechtenstein · Ocrevus
- Norway · Ocrevus
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/e34902f8-9bef-4a97-8733-8f2510eca18f GET /v1/drugs/e34902f8-9bef-4a97-8733-8f2510eca18f?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": "20160427000077",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20160427000077",
"product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/ocrevus"
}See everything about ocrelizumab.
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.