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Ireland· IE-PA-EU/1/17/1184/001-002

Riximyo 100 mg concentrate for solution for infusion

A rituximab product containing rituximab, registered in Ireland by Sandoz GmbH. The same ATC class is registered in 3 of our 19 countries.

ATC L01XC02

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedRiximyo 100 mg concentrate for soluti…ATCL01XC02REGISTER NO.IE-PA-EU/1/17/1184/00…PACKS LISTED1CHECKEDSeptember 28, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about rituximabAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Rituximab is registered in 3 of 19 countries.

Countries holding a registration under ATC L01XC02 (rituximab), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 2 of them publish a price we can compare per daily dose
Search rituximab products by name

Rituximab · ATC L01XC02

3 / 19 countries

  • Belgiumprice
  • Ireland
  • Polandprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

HPRA (Ireland)
Active substance
Rituximab
Manufacturer
Sandoz GmbH
Country
Ireland (IE)
ATC code
L01XC02
ATC class
Rituximab
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/17/1184/001-002

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

81 interactions on record for rituximab.

Graded by severity as the source publishes them — 32 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
Check rituximab against other medicinesHow interaction checks work

Rituximab · interactions on record

81 records

  • 32 severe
  • 42 moderate
  • 7 minor

Most severe, free to view

  • CladribineL01BB04severe
  • Talimogene laherparepvecL01XL02severe
  • Talimogen laherparepvecL01XX51severe
  • LeflunomidL04AA13severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Rituximab in 15 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All rituximab products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Ituxredi
  • Iceland · Blitzima, Mabthera
  • Liechtenstein · Blitzima, Mabthera
  • Norway · Blitzima, Mabthera

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 HPRA (Ireland). 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/ce37d05a-7e44-4d9b-b223-d6187db8bc94
GET /v1/drugs/ce37d05a-7e44-4d9b-b223-d6187db8bc94?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": "Concentrate for solution for infusion",
  "routes": [
    "Intravenous use"
  ],
  "source": "hpra",
  "atc_all": [
    "L01XC",
    "L01XC02"
  ],
  "strength": null,
  "pa_number": "EU/1/17/1184/001-002",
  "substances": [
    "Rituximab"
  ],
  "legal_basis": "Similar biological application (Article 10(4) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "15/06/2017",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}
API referenceMCP serverPlans

See everything about rituximab.

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.

Try it freeOpen in the console