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Netherlands· NL-4254af11d915

Padcev 20 mg, poeder voor oplossing voor infusie

A enfortumab vedotin product containing enfortumab vedotin, registered in Netherlands by Astellas Pharma Europe B.V.. The same ATC class is registered in 13 of our 19 countries.

ATC L01FX13

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedPadcev 20 mg, poeder voor oplossing v…ATCL01FX13REGISTER NO.NL-4254af11d915PACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Enfortumab vedotin is registered in 13 of 19 countries.

Countries holding a registration under ATC L01FX13 (enfortumab vedotin), each read from that country’s own register.

  • This record: Netherlands, from CBG-MEB (Netherlands)
  • 8 of them publish a price we can compare per daily dose

Enfortumab vedotin · ATC L01FX13

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • 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

CBG-MEB (Netherlands)
Active substance
ENFORTUMAB VEDOTIN
Manufacturer
Astellas Pharma Europe B.V.
Country
Netherlands (NL)
ATC code
L01FX13
ATC class
Enfortumab vedotin
Defined daily dose
9.4 mg, P
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/21/1615

Regulatory notes

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

Interactions

190 interactions on record for enfortumab vedotin.

Graded by severity as the source publishes them — 37 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

Enfortumab vedotin · interactions on record

190 records

  • 37 severe
  • 150 moderate
  • 3 minor

Most severe, free to view

  • KetoconazoleH02CA03severe
  • ClarithromycinJ01FA09severe
  • KetoconazoleJ02AB02severe
  • Darunavir and cobicistatJ05AR14severe
  • 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

Enfortumab vedotin in 15 other countries

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

All enfortumab vedotin products

Authorised across Europe · EMA

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

  • Iceland · Padcev
  • Liechtenstein · Padcev
  • Norway · Padcev

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 CBG-MEB (Netherlands). 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/91dec516-9330-4353-8d76-bf92c7205058
GET /v1/drugs/91dec516-9330-4353-8d76-bf92c7205058?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": "Poeder voor oplossing voor infusie",
  "route": "Intraveneus gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/padcev-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Enfortumab vedotin",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp128098",
  "excipients": [
    "HISTIDINE, (L-)",
    "HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
    "POLYSORBAAT 20 (E 432)",
    "STIKSTOF (HEAD SPACE) (E 941)",
    "TREHALOSE (Alpha, Alpha-)  2-WATER"
  ],
  "substances": [
    "ENFORTUMAB VEDOTIN"
  ],
  "leaflet_url": null,
  "authorised_at": "2022/04/13",
  "procedure_number": "EMEA/H/C/005392",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/21/1615",
  "additional_monitoring": "Y"
}

See everything about enfortumab vedotin.

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.