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Ireland· IE-PA-EU/1/23/1766/001

Yorvipath 168 micrograms/0.56 mL solution for injection in pre-filled pen

A palopegteriparatide product containing palopegteriparatide + teriparatide, registered in Ireland by Ascendis Pharma Bone Diseases A/S. The same ATC class is registered in 11 of our 19 countries.

ATC H05AA05

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedYorvipath 168 micrograms/0.56 mL solu…ATCH05AA05REGISTER NO.IE-PA-EU/1/23/1766/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Palopegteriparatide is registered in 11 of 19 countries.

Countries holding a registration under ATC H05AA05 (palopegteriparatide), 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

Palopegteriparatide · ATC H05AA05

11 / 19 countries

  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • 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.

The record

At a glance

HPRA (Ireland)
Active substance
Palopegteriparatide + Teriparatide
Manufacturer
Ascendis Pharma Bone Diseases A/S
Country
Ireland (IE)
ATC code
H05AA05
ATC class
Palopegteriparatide
Defined daily dose
33 mcg, P
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/23/1766/001

Regulatory notes

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

Same medicine, other countries

Palopegteriparatide in 1 other country

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

All palopegteriparatide 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/1d893d25-3b1f-4b5c-b6f2-88312bbe77c6
GET /v1/drugs/1d893d25-3b1f-4b5c-b6f2-88312bbe77c6?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": "Solution for injection in pre-filled pen",
  "routes": [
    "Subcutaneous use"
  ],
  "source": "hpra",
  "atc_all": [
    "H05AA05"
  ],
  "strength": null,
  "pa_number": "EU/1/23/1766/001",
  "substances": [
    "Palopegteriparatide",
    "Teriparatide"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "17/11/2023",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about palopegteriparatide.

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.