Sweden· SE-20240626000037
Emtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris 200 mg/25 mg/25 mg Filmdragerad tablett
A medicinal product containing emtricitabine + tenofovir alafenamide + rilpivirine, registered in Sweden by Viatris Limited.
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Emtricitabine + Tenofovir Alafenamide + Rilpivirine
- Manufacturer
- Viatris Limited
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer20240626000037
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Emtricitabine + tenofovir alafenamide + rilpivirine in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaEMTRICITABINE/RILPIVIRINE/TENOFOVIR ALAFENAMIDE VIATRISVIATRIS LIMITED, Dublin
- FinlandEmtricitabine/Rilpivirine/Tenofovir Alafenamide ViatrisViatris Limited
- IrelandEmtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris 200 mg/25 mg/25 mg film-coated tabletsViatris Limited
- PolandEmtricitabine/Rilpivirine/Tenofovir Alafenamide ViatrisViatris Ltd
- SpainEMTRICITABINA/RILPIVIRINA/TENOFOVIR ALAFENAMIDA VIATRIS 200 MG/25 MG/25 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFGViatris Limited
- NorwayOdefseyAbacus Medicine A/S
- IcelandEmtricitabine/Rilpivirine/Tenofovir Alafenamide ViatrisViatris Limited
- United StatesODEFSEYGilead Sciences, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Emtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris, Odefsey
- Liechtenstein · Emtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris, Odefsey
- Norway · Emtricitabine/Rilpivirine/Tenofovir Alafenamide Viatris, Odefsey
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 Swedish Medical Products Agency (Sweden). 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/d3d797f9-4a78-4295-bd13-f20eeded37fe GET /v1/drugs/d3d797f9-4a78-4295-bd13-f20eeded37fe?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.
{
"source": "lakemedelsverket",
"doc_types": [
"EMA",
"EPAR"
],
"se_npl_id": "20240626000037",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20240626000037",
"product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/emtricitabine-rilpivirine-tenofovir-alafenamide-viatris"
}See everything about emtricitabine + tenofovir alafenamide + rilpivirine.
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.