Sweden· SE-20170203000054
ellaOne 30 mg Filmdragerad tablett
A medicinal product containing ulipristal acetate, registered in Sweden by Laboratoire HRA Pharma.
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
- Ulipristal Acetate
- Manufacturer
- Laboratoire HRA Pharma
- 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_varunummer20170203000054
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ulipristal acetate in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsEcinq 30 mg filmomhulde tablettenAspen Healthcare Malta Limited
- SpainELLAONE 30 MG COMPRIMIDO RECUBIERTO CON PELICULALaboratoire Hra Pharma
- FinlandellaOneParanova Oy
- FranceELLAONE 30 mg, comprimé pelliculéHRA PHARMA
- PolandellaOneLaboratoire HRA Pharma
- CzechiaELLAONELaboratoire HRA Pharma, Chatillon
- IrelandellaOne 30 mg film-coated tabletLaboratoire HRA Pharma
- IcelandellaOneLaboratoire HRA Pharma*
Authorised across Europe · EMA
The same active substance is authorised in 18 EEA countries. Names it is sold under:
- Austria · Lencya, Ulipristal Acetate Hexal
- Czechia · Ulipristal Acetate Aristo
- Germany · Femke, Lencya
- Denmark · Femke, Ulipristal Acetate Stada
- Spain · Ulipristal Aristo, Ulipristal Aurovitas
- Finland · Femke, Ulipristal Acetate Stada
- France · Ulipristal Acetate Biogaran, Ulipristal Acétate Exeltis
- United Kingdom (Northern Ireland) · Contrella, Ellaone
- Greece · Boled, Elperil
- Ireland · Ulipristal Acetate Rowex
- Iceland · Ellaone, Ulipristal Acetate Stada
- Italy · Evante, Lencya
- Liechtenstein · Ellaone
- Malta · Ecinq
- Netherlands · Ecinq, Evante
- Norway · Ellaone, Femke
- Poland · Misstala, Ulipristal Aristo
- Portugal · Femke, Ulipristal Aristo
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/242cd2a6-df70-4588-8263-06d856685b8e GET /v1/drugs/242cd2a6-df70-4588-8263-06d856685b8e?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": [
"EMA",
"EPAR"
],
"se_npl_id": "20170203000054",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20170203000054",
"product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/ellaone"
}See everything about ulipristal acetate.
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.