Ireland· IE-PA-EU/1/13/856/004
Lonquex 6 mg/0.6 ml solution for injection
A lipegfilgrastim product containing lipegfilgrastim, registered in Ireland by Teva B.V.. The same ATC class is registered in 12 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Lipegfilgrastim is registered in 12 of 19 countries.
Countries holding a registration under ATC L03AA14 (lipegfilgrastim), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 8 of them publish a price we can compare per daily dose
Lipegfilgrastim · ATC L03AA14
12 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
The record
At a glance
HPRA (Ireland)- Active substance
- lipegfilgrastim
- Manufacturer
- Teva B.V.
- Country
- Ireland (IE)
- ATC code
- L03AA14
- ATC class
- Lipegfilgrastim
- Defined daily dose
- 0.3 mg, P
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/13/856/004
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Lipegfilgrastim in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaLONQUEXTeva B.V., Haarlem
- SpainLONQUEX 6 MG/0,6 ML SOLUCION INYECTABLETeva B.V.
- IcelandLonquexTeva B.V.*
- NorwayLonquexTeva B.V.
- PolandLonquexTeva B.V.
- BelgiumLonquex 6 mg/0.6 mlTeva
- SwedenLonquex 6 mg/0,6 ml Injektionsvätska, lösningTeva B.V.
- FinlandLonquexParanova Oy
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Lonquex
- Iceland · Lonquex
- Liechtenstein · Lonquex
- Norway · Lonquex
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/14e6b0da-98af-42bc-bfa1-18053908035b GET /v1/drugs/14e6b0da-98af-42bc-bfa1-18053908035b?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",
"routes": null,
"source": "hpra",
"atc_all": [
"L03AA14"
],
"strength": null,
"pa_number": "EU/1/13/856/004",
"substances": [
"lipegfilgrastim"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "19/04/2023",
"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 lipegfilgrastim.
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.