Germany· DE-A57-8429563007bdb8d5
Tetraethylthiuramdisulfid Smartpractice Europe
A disulfiram product containing disulfiram, registered in Germany by Smartpractice Europe Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Disulfiram
- Manufacturer
- Smartpractice Europe Gmbh
- Country
- Germany (DE)
- ATC code
- DISULFIRAM
- ATC class
- DISULFIRAM
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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 in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomAntabuse 200mg tabletsActavis UK Ltd
- United StatesDisulfiramGolden State Medical Supply, Inc.
- SwedenAntabus 200 mg BrustablettActavis Group PTC ehf.
- NorwayAntabusTeva Pharmaceuticals
- CzechiaANTABUSTeva B.V., Haarlem
- PolandAnticolZakłady Farmaceutyczne POLPHARMA S.A.
- NetherlandsAntabus dispergetten 400 mg, bruistablettenAurobindo Pharma B.V.
- 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
- 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
- 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 EMA Article 57 (European Union). 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/77be2f70-674a-4357-b15d-a81afd65f440 GET /v1/drugs/77be2f70-674a-4357-b15d-a81afd65f440?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.
{
"pzn": null,
"route": "Cutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Disulfiram",
"atc_from_source": null,
"authorisation_country": "Germany"
}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.