Germany· DE-A57-9cffe60ba645ab8e
Femke
A medicinal product containing ulipristal acetate, registered in Germany by Exeltis Germany Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Ulipristal Acetate
- Manufacturer
- Exeltis Germany Gmbh
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
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.
- SpainELLAONE 30 MG COMPRIMIDO RECUBIERTO CON PELICULALaboratoire Hra Pharma
- FinlandellaOneParanova Oy
- NetherlandsEcinq 30 mg filmomhulde tablettenAspen Healthcare Malta Limited
- United KingdomEllaOne 30mg tabletsOmega Pharma Ltd
- PolandellaOneLaboratoire HRA Pharma
- BelgiumEllaOne 30 mgLaboratoire HRA Pharma
- CzechiaELLAONELaboratoire HRA Pharma, Chatillon
- FranceELLAONE 30 mg, comprimé pelliculéHRA 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
- 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
- Sweden · Ulipristal Acetate Stada
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 EMA Article 57 (European Union). 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/3e9dcc3f-e28a-4620-8ca0-2d2b5db95fd9 GET /v1/drugs/3e9dcc3f-e28a-4620-8ca0-2d2b5db95fd9?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.
{
"pzn": null,
"route": "Oral Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Ulipristal Acetate",
"atc_from_source": null,
"authorisation_country": "Germany"
}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.