Ireland· IE-PA-EU/1/25/1952/001-002
Emtricitabine/Tenofovir alafenamide Viatris 200 mg/10 mg film-coated tablets
A emtricitabine and tenofovir alafenamide product containing emtricitabine, registered in Ireland by Viatris Limited. The same ATC class is registered in 13 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Emtricitabine and tenofovir alafenamide is registered in 13 of 19 countries.
Countries holding a registration under ATC J05AR17 (emtricitabine and tenofovir alafenamide), 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
Emtricitabine and tenofovir alafenamide · ATC J05AR17
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
HPRA (Ireland)- Active substance
- Emtricitabine
- Manufacturer
- Viatris Limited
- Country
- Ireland (IE)
- ATC code
- J05AR17
- ATC class
- Emtricitabine and tenofovir alafenamide
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/25/1952/001-002
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Emtricitabine and tenofovir alafenamide in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumDescovy 200 mg - 10 mgGilead Sciences Ireland UC
- United StatesemtricitabineCipla USA Inc.
- CzechiaEMTRIVAGilead Sciences Ireland UC, Carrigtohill
- FinlandEmtrivaGilead Sciences Ireland UC
- FranceEMTRIVA 10 mg/ml, solution buvableGILEAD SCIENCES IRELAND UC (IRLANDE)
- United KingdomEmtriva 10mg/ml oral solutionGilead Sciences Ltd
- NetherlandsEmtriva 10 mg/ml, drankGilead Sciences Ireland UC
- IcelandEmtrivaGilead Sciences Ireland UC*
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Spain · Emtricitabina/Tenofovir Alafenamida Dr. Reddys
- Iceland · Emtriva
- Liechtenstein · Emtriva
- Norway · Emtriva
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/3b514550-f8f3-4a14-ad6b-6cd11fbfb627 GET /v1/drugs/3b514550-f8f3-4a14-ad6b-6cd11fbfb627?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": [
"J05AR17"
],
"strength": null,
"pa_number": "EU/1/25/1952/001-002",
"substances": [
"Emtricitabine"
],
"legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "18/07/2025",
"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 emtricitabine and tenofovir alafenamide.
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.