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Ireland· IE-PA-EU/1/10/648/008-014

Twynsta 40 mg/10 mg tablets

A angiotensin ii receptor blockers (arbs), combinations product containing amlodipine besilate + telmisartan, registered in Ireland by Boehringer Ingelheim International GmbH.

ATC C09D

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedTwynsta 40 mg/10 mg tabletsATCC09DREGISTER NO.IE-PA-EU/1/10/648/008…PACKS LISTED1CHECKEDSeptember 28, 2026

The record

At a glance

HPRA (Ireland)
Active substance
Amlodipine besilate + Telmisartan
Manufacturer
Boehringer Ingelheim International GmbH
Country
Ireland (IE)
ATC code
C09D
ATC class
ANGIOTENSIN II RECEPTOR BLOCKERS (ARBs), COMBINATIONS
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/10/648/008-014

Regulatory notes

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

Same medicine, other countries

Amlodipine besilate + telmisartan in 12 other countries

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

All amlodipine besilate + telmisartan products

Authorised across Europe · EMA

The same active substance is authorised in 19 EEA countries. Names it is sold under:

  • Austria · Telmisartan/Amlodipin Krka
  • Bulgaria · Актелсар Дуо, Равентон
  • Czechia · Tamloset, Telassmo
  • Germany · Actelsar Duo, Telmisartan/Amlodipin 089pharm
  • Estonia · Mixor, Teldipin
  • Spain · Telmisartán/Amlodipino Krka, Telmisartán/Amlodipino Teva
  • France · Telmisartan/Amlodipine Arrow
  • Greece · Cardynsta
  • Hungary · Arettan, Cotanydon
  • Iceland · Twynsta
  • Liechtenstein · Twynsta
  • Lithuania · Raventon
  • Latvia · Mixor, Raventon
  • Norway · Twynsta
  • Poland · Telam, Teldipin
  • Portugal · Amlodipina + Telmisartan Generis, Amlodipina + Telmisartan Krka
  • Romania · Telassmo
  • Slovenia · Telassmo
  • Slovakia · Mixor, Teldipin

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/3aa7a5ea-1b44-4acf-9f9c-1fbefa8b043b
GET /v1/drugs/3aa7a5ea-1b44-4acf-9f9c-1fbefa8b043b?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": "Tablet",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "C09D"
  ],
  "strength": null,
  "pa_number": "EU/1/10/648/008-014",
  "substances": [
    "Amlodipine besilate",
    "Telmisartan"
  ],
  "legal_basis": "Fixed combination application (Article 10b of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "07/10/2010",
  "dispensing_status": "Product subject to prescription which may be renewed (B)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about amlodipine besilate + telmisartan.

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.