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Ireland· IE-PA-EU/1/09/545/1-10

Onglyza 5 mg film-coated tablets

A saxagliptin product containing saxagliptin, registered in Ireland by AstraZeneca AB. The same ATC class is registered in 16 of our 19 countries.

ATC A10BH03

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedOnglyza 5 mg film-coated tabletsATCA10BH03REGISTER NO.IE-PA-EU/1/09/545/1-10PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Saxagliptin is registered in 16 of 19 countries.

Countries holding a registration under ATC A10BH03 (saxagliptin), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 10 of them publish a price we can compare per daily dose

Saxagliptin · ATC A10BH03

16 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Italyprice
  • Japan
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
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.

Price per daily dose

What a daily dose of saxagliptin costs, country by country.

Normalised to the WHO defined daily dose (5 mg), the median price runs from $0.31 in France to $3.59 in Italy — a ×12 gap.

  • 3 markets with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Saxagliptin · price per daily dose (5 mg)

USD · FX 28 Sept 2026

  • IT Italy$3.59
  • CH Switzerland$3.41
  • FR France$0.31
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

HPRA (Ireland)
Active substance
Saxagliptin
Manufacturer
AstraZeneca AB
Country
Ireland (IE)
ATC code
A10BH03
ATC class
Saxagliptin
Defined daily dose
5 mg, O
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/09/545/1-10

Regulatory notes

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

Interactions

449 interactions on record for saxagliptin.

Graded by severity as the source publishes them — 3 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

Saxagliptin · interactions on record

449 records

  • 3 severe
  • 404 moderate
  • 42 minor

Most severe, free to view

  • ClotrimazoleA01AB18moderate
  • CimetidineA02BA01moderate
  • SucralfateA02BX02moderate
  • ThiethylperazinA04AB03moderate
  • 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

Saxagliptin in 15 other countries

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

All saxagliptin products

Authorised across Europe · EMA

The same active substance is authorised in 9 EEA countries. Names it is sold under:

  • France · Saxagliptine Arrow, Saxagliptine Biogaran
  • United Kingdom (Northern Ireland) · Saxagliptin Sandoz, Saxagliptin Zydus Pharmaceuticals Uk
  • Hungary · Saxagliptin Pharos
  • Iceland · Onglyza
  • Liechtenstein · Onglyza
  • Malta · Saxagliptin Pharos
  • Netherlands · Saxagliptine Sandoz
  • Norway · Onglyza
  • Portugal · Saxagliptina Generis, Saxagliptina Generis Phar

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/e599002c-35ee-4f90-ab9f-61066d2ccad7
GET /v1/drugs/e599002c-35ee-4f90-ab9f-61066d2ccad7?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": [
    "A10BH",
    "A10BH03"
  ],
  "strength": null,
  "pa_number": "EU/1/09/545/1-10",
  "substances": [
    "Saxagliptin"
  ],
  "legal_basis": "New active substance (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "01/10/2009",
  "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 saxagliptin.

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.