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.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
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
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_idEU/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.
Same medicine, other countries
Teprotumumab in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceTEPEZZA 500 mg, poudre pour solution à diluer pour perfusionAMGEN EUROPE
- United StatesTEPEZZAHorizon Therapeutics USA, Inc.
- SwitzerlandTepezza 500 mg, Pulver für ein Konzentrat zur Herstellung einer InfusionslösungAmgen Switzerland AG
- CzechiaTEPEZZAAmgen Europe B.V., Breda
- SpainTEPEZZA 500 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONAmgen Europe B.V.
- FinlandTEPEZZAAmgen Europe B.V.
- BelgiumTepezza 500 mgAmgen Europe
- IrelandTEPEZZA 500 mg powder for concentrate for solution for infusionAmgen Europe B.V.,
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Iceland · Tepezza
- Norway · Tepezza
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/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.