Sweden· SE-19990413000057
Cetrotide 0,25 mg Pulver och vätska till injektionsvätska, lösning
A medicinal product containing cetrorelix, registered in Sweden by Merck Europe B.V..
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Cetrorelix
- Manufacturer
- Merck Europe B.V.
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer19990413000057
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Cetrorelix in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandCetrorelix Leman 0,25 mg, poudre pour solution injectableLeman SKL SA
- SpainCETRORELIX EDEST 0,25 MG POLVO PARA SOLUCION INYECTABLEIntas Third Party Sales 2005 S.L.
- BelgiumCetrotide 0.25 mgMerck Europe
- United KingdomCetrotide 250microgram powder and solvent for solution for injection vialsMerck Serono Ltd
- IcelandCetrotideMerck Europe B.V.*
- NorwayCetrotideMerck Serono Europe Ltd
- CzechiaCETROTIDEMerck Europe B.V., Amsterdam
- IrelandCetrotide 0.25 mg powder and solvent for solution for injectionMerck Europe B.V.
Authorised across Europe · EMA
The same active substance is authorised in 14 EEA countries. Names it is sold under:
- Belgium · Ceziboe
- Czechia · Cetrorelix Sun, Ceziboe
- Germany · Ceziboe
- Spain · Ceziboe Sun
- France · Ceziboe
- United Kingdom (Northern Ireland) · Ceziboe
- Greece · Ceziboe
- Hungary · Ceziboe
- Ireland · Ceziboe
- Iceland · Cetrotide
- Italy · Ceziboe
- Liechtenstein · Cetrotide
- Netherlands · Ceziboe
- Norway · Cetrotide
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 Swedish Medical Products Agency (Sweden). 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/963f7be3-3d9b-4833-9a89-cc0e3c1e2f11 GET /v1/drugs/963f7be3-3d9b-4833-9a89-cc0e3c1e2f11?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.
{
"source": "lakemedelsverket",
"doc_types": [
"EPAR",
"EMA"
],
"se_npl_id": "19990413000057",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=19990413000057",
"product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/cetrotide-epar-product-information_sv.pdf"
}See everything about cetrorelix.
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.