Netherlands· NL-5898cb820056
Refusal, tabletten 250 mg
A disulfiram product containing disulfiram, registered in Netherlands by ACE Pharmaceuticals B.V.. The same ATC class is registered in 13 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Disulfiram is registered in 13 of 19 countries.
Countries holding a registration under ATC N07BB01 (disulfiram), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 8 of them publish a price we can compare per daily dose
Disulfiram · ATC N07BB01
13 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of disulfiram costs, country by country.
Normalised to the WHO defined daily dose (0.2 g), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Disulfiram · price per daily dose (0.2 g)
USD · FX 28 Sept 2026
- CH Switzerland$0.55
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- DISULFIRAM
- Manufacturer
- ACE Pharmaceuticals B.V.
- Country
- Netherlands (NL)
- ATC code
- N07BB01
- ATC class
- Disulfiram
- Defined daily dose
- 0.2 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id03182
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
210 interactions on record for disulfiram.
Graded by severity as the source publishes them — 19 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Disulfiram · interactions on record
210 records
- 19 severe
- 163 moderate
- 15 minor
- 13 info
Most severe, free to view
- EthanolB05XX04severe
- MipomersenC10AX11severe
- LomitapideC10AX12severe
- MetronidazoleJ01XD01severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Disulfiram in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesDisulfiramBryant Ranch Prepack
- SpainANTABUS 250 mg COMPRIMIDOSLaboratorios Bohm S.A.
- United KingdomAntabuse 250mg tabletsImported (United States)
- NorwayAntabus
- SwedenAntabus 200 mg BrustablettActavis Group PTC ehf.
- CzechiaANTABUSTeva B.V., Haarlem
- PolandAnticolZakłady Farmaceutyczne POLPHARMA S.A.
- BelgiumAntabuse 400 mgSanofi Belgium
Authorised across Europe · EMA
The same active substance is authorised in 17 EEA countries. Names it is sold under:
- Czechia · Antabus
- Germany · Tetraethylthiuramdisulfid Smartpractice Europe
- Denmark · Antabus
- Spain · Antabus
- Finland · Antabus
- France · Esperal
- United Kingdom (Northern Ireland) · Antabuse, Disulfiram Accord-Uk
- Hungary · Antaethyl
- Ireland · Antabuse
- Iceland · Antabus
- Italy · Antabuse Dispergettes, Etiltox
- Malta · Disural
- Norway · Antabus
- Poland · Anticol, Disulfiram Wzf
- Portugal · Tetradin
- Romania · Antalcol
- Sweden · Antabus
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 CBG-MEB (Netherlands). 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/03e600e2-6f20-4c9c-899f-35ad5cd81e08 GET /v1/drugs/03e600e2-6f20-4c9c-899f-35ad5cd81e08?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": "Tablet",
"route": "Oraal gebruik",
"soort": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h03182_smpc.pdf",
"strength": null,
"atc_label": "Disulfiram",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg03182",
"excipients": [
"CROSCARMELLOSE NATRIUM (E 468)",
"LACTOSE 1-WATER",
"MAGNESIUMSTEARAAT (E 470b)",
"MAÏSZETMEEL",
"NATRIUMLAURILSULFAAT",
"TALK (E 553b)",
"ZETMEEL, GEPREGELATINEERD"
],
"substances": [
"DISULFIRAM"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h03182.pdf",
"authorised_at": "1986/03/11",
"procedure_number": null,
"dispensing_status": "Uitsluitend recept",
"registration_number": "03182",
"additional_monitoring": "N"
}See everything about disulfiram.
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.