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Sweden· SE-20191012000080

Pentacarinat 300 mg Pulver till injektions-/infusions-/nebulisatorvätska, lösning

A medicinal product containing pentamidine diisetionate, registered in Sweden by Ebb Medical AB.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedPentacarinat 300 mg Pulver till injek…ATC—REGISTER NO.SE-20191012000080PACKS LISTED1CHECKEDJuly 30, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Pentamidine Diisetionate
Manufacturer
Ebb Medical AB
Country
Sweden (SE)
ATC code
—
Reimbursed
Not published by this register
Source register
Swedish Medical Products Agency (Sweden)
Last checked
July 30, 2026

Packs & prices · 1

  • se_varunummer
    20191012000080

Regulatory notes

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

Same medicine, other countries

Pentamidine diisetionate in 8 other countries

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

All pentamidine diisetionate products

Authorised across Europe · EMA

The same active substance is authorised in 12 EEA countries. Names it is sold under:

  • Belgium · Pentacarinat
  • Germany · Pentacarinat, Pentamidindiisetionat Tillomed
  • Denmark · Pentamidine Tillomed
  • Spain · Pentacarinat
  • Finland · Pentamidine Tillomed
  • France · Pentacarinat, Pentamidine Tillomed
  • United Kingdom (Northern Ireland) · Pentamidine Isetionate Tillomed
  • Ireland · Pentamidine Tillomed
  • Italy · Pentacarinat
  • Luxembourg · Pentacarinat
  • Netherlands · Pentacarinat, Pentamidinediisetionaat Tillomed
  • Norway · Pentamidine Diisetionate Tillomed

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/dbca5715-2528-4a51-b1bf-dafa197d9fa9
GET /v1/drugs/dbca5715-2528-4a51-b1bf-dafa197d9fa9?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": [
    "PL"
  ],
  "se_npl_id": "20191012000080",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20191012000080",
  "product_doc_link": "https://docetp.mpa.se/LMF/Pentacarinat%20300%20mg%20powder%20for%20solution%20for%20injection_infusion_nebuliser%20IT%20PL_09001bee80ae0d12.pdf"
}

See everything about pentamidine diisetionate.

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.