Sweden· SE-19930629000137
Relifex 500 mg Filmdragerad tablett
A medicinal product containing nabumetone, 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
- Nabumetone
- Manufacturer
- Viatris AB
- 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_varunummer19930629000137
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Nabumetone in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesNabumetoneAmerican Health Packaging
- FinlandNabumeton Bmm PharmaBMM Pharma AB
- IrelandNabumetone Tillomed 500 mg Film-coated TabletsTillomed Pharma GmbH
- BelgiumGambaran 500 mgViatris Healthcare
- IcelandRelifexViatris ApS
- NetherlandsMebutan 500 mg, tablettenViatris Healthcare B.V.
- NorwayRelifexViatris AS
- FranceNABUCOM 500 mg, comprimé pelliculéARROW GENERIQUES
Authorised across Europe · EMA
The same active substance is authorised in 17 EEA countries. Names it is sold under:
- Belgium · Gambaran, Nabumeton Tillomed
- Germany · Relifex
- Estonia · Relifex
- Spain · Relif
- France · Nabucom
- United Kingdom (Northern Ireland) · Nabumetone Accord-Uk, Nabumetone Kent Pharma Uk
- Greece · Akratol, Nabuton
- Hungary · Relifex
- Ireland · Nabumetone Tillomed, Relifex
- Iceland · Relifex
- Italy · Nabuser
- Lithuania · Relifex
- Luxembourg · Gambaran
- Latvia · Relifex
- Netherlands · Mebutan, Mebutan Dispers
- Norway · Relifex
- Poland · Nabuton Vp
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/186ca650-406e-4d90-9ee1-b62b26c50e1f GET /v1/drugs/186ca650-406e-4d90-9ee1-b62b26c50e1f?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": "19930629000137",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=19930629000137",
"product_doc_link": "https://docetp.mpa.se/LMF/Relifex%20500%20mg%20film-coated%20tablet%20SmPC_09001bee830235d1.pdf"
}See everything about nabumetone.
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.