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United Kingdom· GB-APID-42526711000001107

Zynlonta 10mg powder for concentrate for solution for infusion vials

A loncastuximab tesirine product containing loncastuximab tesirine, registered in United Kingdom by Swedish Orphan Biovitrum Ltd. The same ATC class is registered in 11 of our 19 countries.

ATC L01FX22

Checked against NHS dm+d (United Kingdom) on

Informational only — not a medical device.

SOURCE REGISTER · GBNHS dm+d (United Kingdom)normalisedZynlonta 10mg powder for concentrate …ATCL01FX22REGISTER NO.GB-APID-4252671100000…PACKS LISTED2CHECKEDSeptember 13, 2026

Where it is registered

Loncastuximab tesirine is registered in 11 of 19 countries.

Countries holding a registration under ATC L01FX22 (loncastuximab tesirine), each read from that country’s own register.

  • This record: United Kingdom, from NHS dm+d (United Kingdom)
  • 7 of them publish a price we can compare per daily dose

Loncastuximab tesirine · ATC L01FX22

11 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • United Kingdom
  • United Statesprice
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

NHS dm+d (United Kingdom)
Active substance
Loncastuximab tesirine
Manufacturer
Swedish Orphan Biovitrum Ltd
Country
United Kingdom (GB)
ATC code
L01FX22
ATC class
Loncastuximab tesirine
Defined daily dose
0.25 mg, P
Reimbursed
Not published by this register
Source register
NHS dm+d (United Kingdom)
Last checked
September 13, 2026

Packs & prices · 2

  • gtin
    7350031444056
  • gtin
    7350031444049

Regulatory notes

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

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of NHS dm+d (United Kingdom). 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/b279dce8-3608-412d-b70b-afb190806e8a
GET /v1/drugs/b279dce8-3608-412d-b70b-afb190806e8a?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.

{
  "apid": "42526711000001107",
  "desc": "Zynlonta 10mg powder for concentrate for solution for infusion vials (Swedish Orphan Biovitrum Ltd)",
  "form": "Powder for solution for infusion",
  "vpid": "42534611000001105",
  "source": "dmd",
  "vtm_id": "1157145002",
  "strength": "10 mg",
  "substance": "Loncastuximab tesirine",
  "ingredient": "Loncastuximab tesirine",
  "supplier_code": "4232111000001108"
}

See everything about loncastuximab tesirine.

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.