Sweden· SE-20000128000092
Teveten 600 mg Filmdragerad tablett
A medicinal product containing eprosartan, registered in Sweden by Viatris AB.
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
- Eprosartan
- Manufacturer
- Viatris AB
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- June 5, 2026
Packs & prices · 1
- se_varunummer20000128000092
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Eprosartan in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainEPROSARTAN MYLAN PHARMACEUTICALS 600 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFGMylan Pharmaceuticals S.L.
- FinlandEprosartan MylanMylan AB
- BelgiumTeveten 600 mgViatris Healthcare
- IrelandTeveten 600 mg film-coated tabletsPCO Manufacturing Ltd.
- NorwayTeveten2care4 ApS
- NetherlandsTeveten 600, filmomhulde tabletten 600 mgViatris Healthcare B.V.
- United KingdomEprosartan 300mg tabletsAmarox Ltd
- GermanyEprosartan AmaroxAmarox Pharma Gmbh
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Teveten
- Belgium · Teveten
- Bulgaria · Теветен
- Germany · Eprosartan Amarox, Eprosartan Ratiopharm
- Spain · Futuran, Navixen
- Finland · Teveten
- United Kingdom (Northern Ireland) · Eprosartan Activase Pharmaceuticals, Eprosartan Amarox
- Greece · Teveten
- Ireland · Teveten
- Luxembourg · Teveten
- Netherlands · Teveten
- Norway · Teveten
- Portugal · Teveten
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/25880671-0712-4123-bb9c-eafafdbe0131 GET /v1/drugs/25880671-0712-4123-bb9c-eafafdbe0131?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": [
"SmPC",
"PL"
],
"se_npl_id": "20000128000092",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20000128000092",
"product_doc_link": "https://docetp.mpa.se/LMF/Teveten%20film-coated%20tablet%20SmPC_09001bee807a7511.pdf"
}See everything about eprosartan.
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.