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Ireland· IE-PA-PA0711/292/001

Ulipristal Acetate Rowex 30 mg film-coated tablets

A ulipristal product containing ulipristal acetate, registered in Ireland by Rowex Limited,. The same ATC class is registered in 11 of our 19 countries.

ATC G03AD02

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedUlipristal Acetate Rowex 30 mg film-c…ATCG03AD02REGISTER NO.IE-PA-PA0711/292/001PACKS LISTED1CHECKEDSeptember 28, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about ulipristal acetateAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Ulipristal is registered in 11 of 19 countries.

Countries holding a registration under ATC G03AD02 (ulipristal), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 7 of them publish a price we can compare per daily dose
Search ulipristal products by name

Ulipristal · ATC G03AD02

11 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

HPRA (Ireland)
Active substance
Ulipristal acetate
Manufacturer
Rowex Limited,
Country
Ireland (IE)
ATC code
G03AD02
ATC class
Ulipristal
Defined daily dose
30 mg, O
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA0711/292/001

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

98 interactions on record for ulipristal.

Graded by severity as the source publishes them — 2 severe. 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
Check ulipristal against other medicinesHow interaction checks work

Ulipristal · interactions on record

98 records

  • 2 severe
  • 77 moderate
  • 19 minor

Most severe, free to view

  • EdoxabanB01AF03severe
  • VenetoclaxL01XX52severe
  • NaldemedineA06AH05moderate
  • RifaximinA07AA11moderate
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Ulipristal in 16 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All ulipristal 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
  • 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 HPRA (Ireland). 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/bbc30e8e-ca37-410e-885a-177603526d34
GET /v1/drugs/bbc30e8e-ca37-410e-885a-177603526d34?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": "Film-coated tablet",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "G03AD",
    "G03AD02"
  ],
  "strength": null,
  "pa_number": "PA0711/292/001",
  "substances": [
    "Ulipristal acetate"
  ],
  "legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
  "market_info": "Marketed",
  "authorised_at": "01/11/2019",
  "dispensing_status": "Product not subject to medical prescription",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": "IC0154-033-014"
}
API referenceMCP serverPlans

See everything about ulipristal.

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.

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