United States· US:50242-150_00b80381-c728-47a0-bd9e-b1223a1c0a40
OCREVUS
A ocrelizumab product containing ocrelizumab, registered in United States by Genentech, Inc.. The same ATC class is registered in 13 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Ocrelizumab is registered in 13 of 19 countries.
Countries holding a registration under ATC L04AG08 (ocrelizumab), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 8 of them publish a price we can compare per daily dose
Ocrelizumab · ATC L04AG08
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of ocrelizumab costs, country by country.
Normalised to the WHO defined daily dose (3.29 mg), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Ocrelizumab · price per daily dose (3.29 mg)
USD · FX 28 Sept 2026
- CH Switzerland$54.58
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- OCRELIZUMAB
- Manufacturer
- Genentech, Inc.
- Country
- United States (US)
- ATC code
- L04AG08
- ATC class
- Ocrelizumab
- Defined daily dose
- 3.29 mg, P
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1150242150011 VIAL, SINGLE-USE in 1 CARTON (50242-150-01) / 10 mL in 1 VIAL, SINGLE-USE
- ndc1150242-150-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
328 interactions on record for ocrelizumab.
Graded by severity as the source publishes them — 27 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Ocrelizumab · interactions on record
328 records
- 27 severe
- 294 moderate
- 7 minor
Most severe, free to view
- CladribineL01BB04severe
- PrednisoloneA07EA01moderate
- HydrocortisoneA07EA02moderate
- PrednisoneA07EA03moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
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.
- FinlandOcrevusOrifarm Oy
- United KingdomOcrevus 300mg/10ml concentrate for solution for infusion vialsRoche Products Ltd
- CzechiaOCREVUSRoche Registration GmbH, Grenzach-Wyhlen
- FranceOCREVUS 300 mg, solution à diluer pour perfusionROCHE REGISTRATION (ALLEMAGNE)
- SwedenOcrevus 300 mg Koncentrat till infusionsvätska, lösningRoche Registration GmbH
- SwitzerlandOcrevus subkutan 920 mg/23 ml, InjektionslösungRoche Pharma (Schweiz) AG
- SpainOCREVUS 300 MG CONCENTRADO PARA SOLUCION PARA PERFUSIONRoche Registration Gmbh
- PolandOcrevusRoche Registration GmbH
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 FDA National Drug Code directory (United States). 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/f4be5e0b-e722-4371-a928-75e991539534 GET /v1/drugs/f4be5e0b-e722-4371-a928-75e991539534?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.
{
"route": "INTRAVENOUS",
"source": "ndc",
"strength": "300",
"substance": "OCRELIZUMAB",
"productndc": "50242-150",
"dosage_form": "INJECTION",
"dea_schedule": null,
"strength_unit": "mg/10mL",
"application_number": "BLA761053",
"marketing_category": "BLA"
}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.