Iceland· IS-IS/1/25/156/01
Tenutex
A disulfiram, kombinationen product containing disulfiramum inn,benzylis benzoas, registered in Iceland by Bioglan AB. The same ATC class is registered in 3 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Disulfiram, kombinationen is registered in 3 of 19 countries.
Countries holding a registration under ATC P03AA54 (disulfiram, kombinationen), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 3 of them publish a price we can compare per daily dose
Disulfiram, kombinationen · ATC P03AA54
3 / 19 countries
- Finlandprice
- Icelandprice
- Norwayprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Disulfiramum INN,Benzylis benzoas
- Manufacturer
- Bioglan AB
- Country
- Iceland (IS)
- ATC code
- P03AA54
- ATC class
- Disulfiram, Kombinationen
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Disulfiram, kombinationen in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandTenutexBioglan AB
- NorwayTenutexBioglan AB
- SwedenTenutex 20 mg/g + 225 mg/g Kutan emulsionBioglan AB
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Finland · Tenutex
- Sweden · Tenutex
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 Icelandic Medicines Agency (Iceland). 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/683d65c7-92e5-4eb1-a5db-8afeb532068c GET /v1/drugs/683d65c7-92e5-4eb1-a5db-8afeb532068c?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.
{
"form": "Húðfleyti",
"source": "lyfjastofnun",
"atc_raw": "P03AA54",
"marketed": false,
"strength": "20 mg/g + 225 mg/g",
"ma_number": "IS/1/25/156/01",
"substance": "Disulfiramum INN,Benzylis benzoas",
"other_info": null,
"legal_status": "(L) Ekki lyfseðilsskylt",
"ma_issued_serial": "46009"
}See everything about disulfiram, kombinationen.
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.