Spain· ES:12723
ANTABUS 250 mg COMPRIMIDOS
A medicinal product containing disulfiram, registered in Spain by Laboratorios Bohm S.A..
Checked against AEMPS CIMA (Spain) on
Informational only — not a medical device.
The record
At a glance
AEMPS CIMA (Spain)- Active substance
- disulfiram
- Manufacturer
- Laboratorios Bohm S.A.
- Country
- Spain (ES)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- AEMPS CIMA (Spain)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cima_codigo70068140EUR 8.41
Regulatory notes
No shortage, Orange Book or US label notes for this record.
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 StatesDisulfiramAlvogen Inc.
- United KingdomAntabuse 250mg tabletsImported (United States)
- NetherlandsRefusal, tabletten 250 mgACE Pharmaceuticals B.V.
- NorwayAntabus
- SwedenAntabus 200 mg BrustablettActavis Group PTC ehf.
- CzechiaANTABUSActavis Group PTC ehf., Hafnarfjördur
- PolandAnticolZakłady Farmaceutyczne POLPHARMA S.A.
- ItalyETILTOX*30 cpr 200 mgMOLTENI & C. F.LLI ALITTI SpA
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
- Finland · Antabus
- France · Esperal
- United Kingdom (Northern Ireland) · Antabuse, Disulfiram Accord-Uk
- Hungary · Antaethyl
- Ireland · Antabuse
- Iceland · Antabus
- Italy · Antabuse Dispergettes, Etiltox
- Malta · Disural
- Netherlands · Disulfiram Aurobindo, Refusal
- 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 AEMPS CIMA (Spain). 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/b2c3e2de-3ec5-4a5e-912c-a46dc6485401 GET /v1/drugs/b2c3e2de-3ec5-4a5e-912c-a46dc6485401?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.
{
"cpresc": "Medicamento Sujeto A Prescripción Médica",
"estado": "{\"aut\":-639108000000}",
"nregistro": "12723",
"substance": "disulfiram"
}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.