Denmark· DK-28105866316
Bunalict
A buprenorphin, kombinationen product containing buprenorphinhydrochlorid, naloxonhydrochloriddihydrat, registered in Denmark by Sandoz A/S. The same ATC class is registered in 10 of our 19 countries.
Checked against Danish Medicines Agency (Denmark) on
Informational only — not a medical device.
Where it is registered
Buprenorphin, kombinationen is registered in 10 of 19 countries.
Countries holding a registration under ATC N07BC51 (buprenorphin, kombinationen), each read from that country’s own register.
- This record: Denmark, from Danish Medicines Agency (Denmark)
- 6 of them publish a price we can compare per daily dose
Buprenorphin, kombinationen · ATC N07BC51
10 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
The record
At a glance
Danish Medicines Agency (Denmark)- Active substance
- BUPRENORPHINHYDROCHLORID, NALOXONHYDROCHLORIDDIHYDRAT
- Manufacturer
- Sandoz A/S
- Country
- Denmark (DK)
- ATC code
- N07BC51
- ATC class
- Buprenorphin, Kombinationen
- Defined daily dose
- 8 mg, SL
- Reimbursed
- Not published by this register
- Source register
- Danish Medicines Agency (Denmark)
- Last checked
- September 30, 2026
Packs & prices · 1
- dk_varenummer28105866316
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under N07BC51
Buprenorphin, kombinationen, as other registers publish it.
- IrelandBulexin 2 mg/0.5 mg sublingual tabletsPinewood Laboratories Limited
- IrelandBulexin 4 mg/1 mg sublingual tabletsPinewood Laboratories Limited
- IrelandBulexin 8 mg/2 mg sublingual tabletsPinewood Laboratories Limited
- DenmarkBunalictSandoz A/S
- FinlandBunalictSandoz A/S
- FinlandBunalictSandoz A/S
- NorwayBunalictSandoz - København
- NorwayBunalictSandoz - København
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Danish Medicines Agency (Denmark). 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/bb9f806b-9842-4eb1-9be4-f97c6579986d GET /v1/drugs/bb9f806b-9842-4eb1-9be4-f97c6579986d?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": "resoribletter, sublinguale",
"source": "dkma",
"strength": "8+2 mg",
"auth_role": "CMS",
"dk_drugid": "28105866316",
"substance": "BUPRENORPHINHYDROCHLORID, NALOXONHYDROCHLORIDDIHYDRAT",
"auth_procedure": "Decentral procedure",
"in_medicinpriser": true,
"registration_date_serial": "43021"
}See everything about buprenorphin, 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.