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France· FR:68852725

IMDYLLTRA 10 mg, poudre pour solution à diluer et solution pour solution pour perfusion

A tarlatamab product containing tarlatamab, registered in France by AMGEN EUROPE. The same ATC class is registered in 12 of our 19 countries.

ATC L01FX33

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedIMDYLLTRA 10 mg, poudre pour solution…ATCL01FX33REGISTER NO.FR:68852725PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Tarlatamab is registered in 12 of 19 countries.

Countries holding a registration under ATC L01FX33 (tarlatamab), each read from that country’s own register.

  • This record: France, from Base de données publique des médicaments — BDPM (France)
  • 7 of them publish a price we can compare per daily dose

Tarlatamab · ATC L01FX33

12 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Japan
  • Netherlands
  • Norwayprice
  • Switzerlandprice
  • United Kingdom
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

Base de données publique des médicaments — BDPM (France)
Active substance
TARLATAMAB
Manufacturer
AMGEN EUROPE
Country
France (FR)
ATC code
L01FX33
ATC class
Tarlatamab
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400955114598
    1 flacon en verre de 10 mg de poudre + 2 flacons en verre de 7 mL de solution

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 Base de données publique des médicaments — BDPM (France). 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/ce7c0574-4504-40cb-a8c2-96682a26b696
GET /v1/drugs/ce7c0574-4504-40cb-a8c2-96682a26b696?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.

{
  "cis": "68852725",
  "date_amm": "2026-05-29",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/26/2033",
  "substance": "TARLATAMAB",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "poudre à diluer à diluer et  solution pour solution pour solution",
  "voies_administration": "intraveineuse",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Oui"
}

See everything about tarlatamab.

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.