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Netherlands· NL-d8fc1c2b8bbb

TEPEZZA 500 mg poeder voor concentraat voor oplossing voor infusie

A teprotumumab product containing teprotumumab, registered in Netherlands by Amgen Europe B.V.. The same ATC class is registered in 10 of our 19 countries.

ATC L04AG13

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedTEPEZZA 500 mg poeder voor concentraa…ATCL04AG13REGISTER NO.NL-d8fc1c2b8bbbPACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Teprotumumab is registered in 10 of 19 countries.

Countries holding a registration under ATC L04AG13 (teprotumumab), each read from that country’s own register.

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

Teprotumumab · ATC L04AG13

10 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Japan
  • Netherlands
  • Polandprice
  • Switzerlandprice
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
TEPROTUMUMAB
Manufacturer
Amgen Europe B.V.
Country
Netherlands (NL)
ATC code
L04AG13
ATC class
Teprotumumab
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/25/1941

Regulatory notes

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

Interactions

55 interactions on record for teprotumumab.

Graded by severity as the source publishes them — 55 moderate. 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

Teprotumumab · interactions on record

55 records

  • 55 moderate

Most severe, free to view

  • LiraglutidA08AX02moderate
  • SemaglutidA08AX03moderate
  • Insulin (human)A10AB01moderate
  • Insulin lisproA10AB04moderate
  • 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.

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/b78cdef5-44b4-4a06-945a-fe00c96ecb50
GET /v1/drugs/b78cdef5-44b4-4a06-945a-fe00c96ecb50?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 concentraat voor oplossing voor infusie",
  "route": "Intraveneus gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/tepezza-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Teprotumumab",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp133459",
  "excipients": [
    "HISTIDINE, (L-)",
    "HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
    "POLYSORBAAT 20 (E 432)",
    "TREHALOSE (Alpha, Alpha-)  2-WATER"
  ],
  "substances": [
    "TEPROTUMUMAB"
  ],
  "leaflet_url": null,
  "authorised_at": "2025/06/19",
  "procedure_number": "EMEA/H/C/006396",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/25/1941",
  "additional_monitoring": "Y"
}

See everything about teprotumumab.

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.