Germany· DE-A57-6fd4f705b76220d3
Melperone Ratiopharm
A melperone product containing melperone hydrochloride, registered in Germany by Ratiopharm Gmbh. The same ATC class is registered in 7 of our 19 countries.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
Where it is registered
Melperone is registered in 7 of 19 countries.
Countries holding a registration under ATC N05AD03 (melperone), each read from that country’s own register.
- This record: Germany, from EMA Article 57 (European Union)
- 4 of them publish a price we can compare per daily dose
Melperone · ATC N05AD03
7 / 19 countries
- Czechiaprice
- Denmark
- Finlandprice
- Germany
- Icelandprice
- Norwayprice
- United Kingdom
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Melperone Hydrochloride
- Manufacturer
- Ratiopharm Gmbh
- Country
- Germany (DE)
- ATC code
- N05AD03
- ATC class
- Melperone
- Defined daily dose
- 0.3 g, O
- 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
Melperone in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandBuronilOvation Healthcare International Ltd.
- United KingdomMelperon-ratiopharm 25mg tabletsImported (Germany)
- NorwayBuronilMedLink A/S
- CzechiaBURONILEQL Pharma AB, Lund
- SwedenBuronil 25 mg Filmdragerad tablettEQL Pharma AB
- IcelandBuronilEQL Pharma AB
- BelgiumMelphalan Tillomed 50 mgTillomed Pharma
Authorised across Europe · EMA
The same active substance is authorised in 9 EEA countries. Names it is sold under:
- Austria · Buronil
- Czechia · Buronil
- Denmark · Buronil
- Estonia · Buronil
- Iceland · Buronil
- Lithuania · Buronil
- Latvia · Buronil
- Portugal · Bunil
- Sweden · Buronil
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/b846d573-7368-4f84-bd1e-f078ef23ae67 GET /v1/drugs/b846d573-7368-4f84-bd1e-f078ef23ae67?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": "Oral Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Melperone Hydrochloride",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about melperone.
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.