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Ireland· IE-PA-EU/1/18/1266/007-012

Steglujan 15 mg/100 mg film-coated tablets

A sitagliptin and ertugliflozin product containing ertugliflozin l-pyroglutamic acid + sitagliptin phosphate monohydrate, registered in Ireland by Merck Sharp & Dohme BV. The same ATC class is registered in 10 of our 19 countries.

ATC A10BD24

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedSteglujan 15 mg/100 mg film-coated ta…ATCA10BD24REGISTER NO.IE-PA-EU/1/18/1266/00…PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Sitagliptin and ertugliflozin is registered in 10 of 19 countries.

Countries holding a registration under ATC A10BD24 (sitagliptin and ertugliflozin), 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

Sitagliptin and ertugliflozin · ATC A10BD24

10 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Italyprice
  • Netherlands
  • 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
Ertugliflozin l-pyroglutamic acid + Sitagliptin phosphate monohydrate
Manufacturer
Merck Sharp & Dohme BV
Country
Ireland (IE)
ATC code
A10BD24
ATC class
Sitagliptin and ertugliflozin
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/18/1266/007-012

Regulatory notes

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

Same medicine, other countries

Sitagliptin and ertugliflozin in 2 other countries

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

All sitagliptin and ertugliflozin 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/b491802f-9968-4759-99c2-cb168899d810
GET /v1/drugs/b491802f-9968-4759-99c2-cb168899d810?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",
    "A10BD24"
  ],
  "strength": null,
  "pa_number": "EU/1/18/1266/007-012",
  "substances": [
    "Ertugliflozin l-pyroglutamic acid",
    "Sitagliptin phosphate monohydrate"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "23/03/2018",
  "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 sitagliptin and ertugliflozin.

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.