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Ireland· IE-PA-EU/1/13/842/01-09

Incresync 12.5 mg/30 mg film-coated tablets

A pioglitazone and alogliptin product containing alogliptin (as benzoate) + pioglitazone (as hydrochloride), registered in Ireland by Takeda Pharma A/S. The same ATC class is registered in 9 of our 19 countries.

ATC A10BD09

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedIncresync 12.5 mg/30 mg film-coated t…ATCA10BD09REGISTER NO.IE-PA-EU/1/13/842/01-…PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Pioglitazone and alogliptin is registered in 9 of 19 countries.

Countries holding a registration under ATC A10BD09 (pioglitazone and alogliptin), 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

Pioglitazone and alogliptin · ATC A10BD09

9 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Italyprice
  • Netherlands
  • 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
Alogliptin (as benzoate) + Pioglitazone (as hydrochloride)
Manufacturer
Takeda Pharma A/S
Country
Ireland (IE)
ATC code
A10BD09
ATC class
Pioglitazone and alogliptin
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/13/842/01-09

Regulatory notes

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

Same medicine, other countries

Pioglitazone and alogliptin in 3 other countries

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

All pioglitazone and alogliptin products

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/24b11f19-e52a-454d-9f8e-5df484528662
GET /v1/drugs/24b11f19-e52a-454d-9f8e-5df484528662?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": [
    "A10BD",
    "A10BD09"
  ],
  "strength": null,
  "pa_number": "EU/1/13/842/01-09",
  "substances": [
    "Alogliptin (as benzoate)",
    "Pioglitazone (as hydrochloride)"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "19/09/2013",
  "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 pioglitazone and alogliptin.

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.