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Ireland· IE-PA-EU/1/21/1570/001

MINJUVI 200 mg powder for concentrate for solution for infusion

A tafasitamab product containing tafasitamab, registered in Ireland by Incyte Biosciences Distribution B.V..

ATC L01XC35

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedMINJUVI 200 mg powder for concentrate…ATCL01XC35REGISTER NO.IE-PA-EU/1/21/1570/001PACKS LISTED1CHECKEDSeptember 28, 2026

The record

At a glance

HPRA (Ireland)
Active substance
Tafasitamab
Manufacturer
Incyte Biosciences Distribution B.V.
Country
Ireland (IE)
ATC code
L01XC35
ATC class
Tafasitamab
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/21/1570/001

Regulatory notes

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

Interactions

58 interactions on record for tafasitamab.

Graded by severity as the source publishes them — 28 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

Tafasitamab · interactions on record

58 records

  • 28 severe
  • 30 moderate

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

Tafasitamab in 15 other countries

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

All tafasitamab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Minjuvi
  • Liechtenstein · Minjuvi
  • Norway · Minjuvi

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/6b06011f-488b-4fba-9a67-f2e9e25b1bc1
GET /v1/drugs/6b06011f-488b-4fba-9a67-f2e9e25b1bc1?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",
  "routes": [
    "Intravenous use"
  ],
  "source": "hpra",
  "atc_all": [
    "L01XC",
    "L01XC35"
  ],
  "strength": null,
  "pa_number": "EU/1/21/1570/001",
  "substances": [
    "Tafasitamab"
  ],
  "legal_basis": "Known active substance (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "26/08/2021",
  "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
}

See everything about tafasitamab.

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.