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Sweden· SE-20171017000018

Ulipristal acetate STADA 30 mg Filmdragerad tablett

A medicinal product containing ulipristal acetate, registered in Sweden by STADA Arzneimittel AG.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedUlipristal acetate STADA 30 mg Filmdr…ATC—REGISTER NO.SE-20171017000018PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Ulipristal Acetate
Manufacturer
STADA Arzneimittel AG
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_varunummer
    20171017000018

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.

All ulipristal acetate products

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/d8dd33a7-6a38-46f3-b1c5-1ca3385d2966
GET /v1/drugs/d8dd33a7-6a38-46f3-b1c5-1ca3385d2966?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": [
    "SmPC",
    "PL"
  ],
  "se_npl_id": "20171017000018",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20171017000018",
  "product_doc_link": "https://docetp.mpa.se/LMF/Ulipristal%20acetate%20STADA%20film-coated%20tablet%20SmPC_09001bee807a6bbb.pdf"
}

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.