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Czechia· CZ-0286359

EMTRICITABINE/TENOFOVIR ALAFENAMIDE VIATRIS

A emtricitabine and tenofovir alafenamide product containing emtricitabine + tenofovir alafenamide monofumarate, registered in Czechia by VIATRIS LIMITED, Dublin. The same ATC class is registered in 13 of our 19 countries.

ATC J05AR17

Checked against SÚKL (Czech Republic) on

Informational only — not a medical device.

SOURCE REGISTER · CZSÚKL (Czech Republic)normalisedEMTRICITABINE/TENOFOVIR ALAFENAMIDE V…ATCJ05AR17REGISTER NO.CZ-0286359PACKS LISTED0CHECKEDSeptember 28, 2026

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: Czechia, from SÚKL (Czech Republic)
  • 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
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

SÚKL (Czech Republic)
Active substance
EMTRICITABINE + TENOFOVIR ALAFENAMIDE MONOFUMARATE
Manufacturer
VIATRIS LIMITED, Dublin
Country
Czechia (CZ)
ATC code
J05AR17
ATC class
Emtricitabine and tenofovir alafenamide
Reimbursed
Not published by this register
Source register
SÚKL (Czech Republic)
Last checked
September 28, 2026

Packs & prices · 0

No packs listed by the register for this record.

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 SÚKL (Czech Republic). 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/ae8d5dea-47af-4b13-88bd-c677b99b3a3c
GET /v1/drugs/ae8d5dea-47af-4b13-88bd-c677b99b3a3c?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": "TBL FLM",
  "source": "sukl",
  "strength": "200MG/25MG",
  "pack_size": "90",
  "substance": "EMTRICITABINE + TENOFOVIR ALAFENAMIDE MONOFUMARATE",
  "cz_kod_sukl": "0286359",
  "product_type": "CH",
  "substance_codes": "15579,4599",
  "registration_state": "R",
  "registration_number": "EU/1/25/1952/008"
}

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.