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Ireland· IE-PA-EU/1/18/1334/001

Vaborem 1 g/1 g powder for concentrate for solution for infusion

A meropenem and vaborbactam product containing vaborbactam + meropenem + meropenem trihydrate, registered in Ireland by Menarini International Operations Luxembourg S.A.. The same ATC class is registered in 13 of our 19 countries.

ATC J01DH52

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedVaborem 1 g/1 g powder for concentrat…ATCJ01DH52REGISTER NO.IE-PA-EU/1/18/1334/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Meropenem and vaborbactam is registered in 13 of 19 countries.

Countries holding a registration under ATC J01DH52 (meropenem and vaborbactam), each read from that country’s own register.

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

Meropenem and vaborbactam · ATC J01DH52

13 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Spainprice
  • 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
VABORBACTAM + Meropenem + Meropenem Trihydrate
Manufacturer
Menarini International Operations Luxembourg S.A.
Country
Ireland (IE)
ATC code
J01DH52
ATC class
Meropenem and vaborbactam
Defined daily dose
3 g, P
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/18/1334/001

Regulatory notes

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

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/8221674d-0099-4c2f-aaa3-d2d48f6b837f
GET /v1/drugs/8221674d-0099-4c2f-aaa3-d2d48f6b837f?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": "Powder for concentrate for solution for infusion",
  "routes": [
    "Intravenous use"
  ],
  "source": "hpra",
  "atc_all": [
    "J01DH52"
  ],
  "strength": null,
  "pa_number": "EU/1/18/1334/001",
  "substances": [
    "VABORBACTAM",
    "Meropenem",
    "Meropenem Trihydrate"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "20/11/2018",
  "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 meropenem and vaborbactam.

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.