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Sweden· SE-19900928000015

Bezalip 200 mg Filmdragerad tablett

A medicinal product containing bezafibrate, registered in Sweden by Actavis Group PTC ehf..

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedBezalip 200 mg Filmdragerad tablettATC—REGISTER NO.SE-19900928000015PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Bezafibrate
Manufacturer
Actavis Group PTC ehf.
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_varunummer
    19900928000015

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Bezafibrate in 11 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All bezafibrate products

Authorised across Europe · EMA

The same active substance is authorised in 14 EEA countries. Names it is sold under:

  • Austria · Bezalip Retard, Bezastad
  • Belgium · Cedur, Eulitop
  • Cyprus · Lacromid, Zafibral
  • Germany · Bezafibrat Al, Bezafibrat Retard Al
  • Spain · Eulitop, Eulitop Retard
  • Finland · Bezalip
  • France · Befizal, Befizal L.P.
  • United Kingdom (Northern Ireland) · Bezafibrate, Bezafibrate Noumed Life Sciences
  • Hungary · Bezalip
  • Italy · Bezalip
  • Luxembourg · Cedur, Eulitop
  • Netherlands · Bezafibrate Aurobindo
  • Portugal · Bezalip, Bezalip Retard
  • Romania · Bezafibrat Arena

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/75beac9a-0924-4d9f-a17f-41398a3df9b9
GET /v1/drugs/75beac9a-0924-4d9f-a17f-41398a3df9b9?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": "19900928000015",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=19900928000015",
  "product_doc_link": "https://docetp.mpa.se/LMF/Bezalip%20film-coated%20tablet%20SmPC_09001bee807a118c.pdf"
}

See everything about bezafibrate.

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.