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Ireland· IE-PA-PA0711/317/001

Solifenacin succinate/Tamsulosin hydrochloride Rowex 6 mg/0.4 mg modified-release tablets

A tamsulosin und solifenacin product containing solifenacin succinate + tamsulosin hydrochloride, registered in Ireland by Rowex Limited,. The same ATC class is registered in 9 of our 19 countries.

ATC G04CA53

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedSolifenacin succinate/Tamsulosin hydr…ATCG04CA53REGISTER NO.IE-PA-PA0711/317/001PACKS LISTED1CHECKEDSeptember 28, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about solifenacin succinate + tamsulosin hydrochlorideAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Tamsulosin und solifenacin is registered in 9 of 19 countries.

Countries holding a registration under ATC G04CA53 (tamsulosin und solifenacin), each read from that country’s own register.

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

Tamsulosin und solifenacin · ATC G04CA53

9 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
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
Solifenacin succinate + Tamsulosin hydrochloride
Manufacturer
Rowex Limited,
Country
Ireland (IE)
ATC code
G04CA53
ATC class
Tamsulosin und Solifenacin
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA0711/317/001

Regulatory notes

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

Same medicine, other countries

Tamsulosin und solifenacin in 10 other countries

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

All tamsulosin und solifenacin products

Authorised across Europe · EMA

The same active substance is authorised in 28 EEA countries. Names it is sold under:

  • Austria · Solicomp, Solifenacin/Tamsulosin Stada
  • Belgium · Solifenacine / Tamsulosine Eurogenerics, Solifenacine/Tamsulosine
  • Bulgaria · Везира, Везомни
  • Cyprus · Nefilin
  • Czechia · Beplasot, Jomil
  • Germany · Solifenacin/Tamsulosin Heumann, Solifenacin/Tamsulosin Ratiopharm
  • Denmark · Solifenacin/Tamsulosin Adalvo, Solifenacin/Tamsulosin Newbury
  • Estonia · Solitombo
  • Spain · Blobax, Daital
  • Finland · Solifenacin/Tamsulosin Stada, Urizia
  • France · Vecalmys
  • United Kingdom (Northern Ireland) · Solifenacin Succinate/Tamsulosin Hydrochloride Altair Science, Solifenacin Succinate/Tamsulosin Hydrochloride Altair Science Limited
  • Greece · Desoltam, Nefilin
  • Croatia · Beplasot, Semquest
  • Hungary · Mingerlan, Örgunderin
  • Iceland · Soltamcin
  • Italy · Luracin, Solifenacina E Tamsulosin Mylan
  • Lithuania · Solitombo
  • Luxembourg · Solifenacine/Tamsulosine, Solifenacine/Tamsulosine Eurogenerics
  • Malta · Jomil
  • Netherlands · Jomil, Mingerlan
  • Norway · Solifenacin/Tamsulosin Newbury, Solifenacin/Tamsulosin Stada
  • Poland · Beplasot, Mingerlan
  • Portugal · Blatan, Solifenacina + Tansulosina Generis
  • Romania · Mingerlan, Solifenacin/Tamsulosin Gemax Pharma
  • Sweden · Urizia
  • Slovenia · Semquest, Solifenacin/Tamsulozin Belupo
  • Slovakia · Jomil, Solifenacín/Tamsulozín Belupo

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/cc69c536-4455-4fb6-92c2-eb4355cfee4b
GET /v1/drugs/cc69c536-4455-4fb6-92c2-eb4355cfee4b?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": "Modified-release tablet",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "G04CA53"
  ],
  "strength": null,
  "pa_number": "PA0711/317/001",
  "substances": [
    "Solifenacin succinate",
    "Tamsulosin hydrochloride"
  ],
  "legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
  "market_info": "Not marketed",
  "authorised_at": "26/05/2023",
  "dispensing_status": "Product subject to prescription which may be renewed (B)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": "IC0101-154-021"
}
API referenceMCP serverPlans

See everything about tamsulosin und solifenacin.

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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