Iceland· IS-EU/1/15/1023/001-003
Farydak
A panobinostat product containing panobinostatum inn, registered in Iceland by Pharmaand GmbH. The same ATC class is registered in 10 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Panobinostat is registered in 10 of 19 countries.
Countries holding a registration under ATC L01XH03 (panobinostat), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 7 of them publish a price we can compare per daily dose
Panobinostat · ATC L01XH03
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Panobinostatum INN
- Manufacturer
- Pharmaand GmbH
- Country
- Iceland (IS)
- ATC code
- L01XH03
- ATC class
- Panobinostat
- Defined daily dose
- 5.7 mg, O
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 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.
Interactions
586 interactions on record for panobinostat.
Graded by severity as the source publishes them — 388 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
Panobinostat · interactions on record
586 records
- 388 severe
- 193 moderate
- 5 minor
Most severe, free to view
- PapaverineA03AD01severe
- CisaprideA03FA02severe
- OndansetronA04AA01severe
- GranisetronA04AA02severe
- 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
Panobinostat in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaFARYDAKpharmaand GmbH, Vienna
- SwitzerlandFarydak 10 mg, Hartkapselnmmpharm GmbH
- FinlandFarydakpharmaand GmbH
- FranceFARYDAK 10 mg, gélulePHARMAAND (AUTRICHE)
- United KingdomFarydak 10mg capsulespharmaand GmbH
- IrelandFarydak 10 mg hard capsulespharmaand GmbH
- NetherlandsFarydak 10 mg harde capsuleszr pharma& GmbH
- NorwayFarydakpharmaand GmbH
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Liechtenstein · Farydak
- Norway · Farydak
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 Icelandic Medicines Agency (Iceland). 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/e5a99609-d345-4b3f-a38d-6dd52923ab2c GET /v1/drugs/e5a99609-d345-4b3f-a38d-6dd52923ab2c?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": "Hart hylki",
"source": "lyfjastofnun",
"atc_raw": "L01XH03",
"marketed": false,
"strength": "10 mg",
"ma_number": "EU/1/15/1023/001-003",
"substance": "Panobinostatum INN",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í krabbameinslækningum.\r\nMarkaðssetning á Íslandi er háð því að Lyfjastofnun hafi staðfest að sérstök skilyrði er varða öryggi og verkun við notkun lyfsins séu uppfyllt.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "42244"
}See everything about panobinostat.
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.