Belgium· BE-AMP-SAM526702-00
Fotivda 890 µg
A tivozanib product containing tivozanib hydrochloride monohydrate, registered in Belgium by Recordati Netherlands. The same ATC class is registered in 10 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Tivozanib is registered in 10 of 19 countries.
Countries holding a registration under ATC L01EK03 (tivozanib), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 7 of them publish a price we can compare per daily dose
Tivozanib · ATC L01EK03
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Tivozanib Hydrochloride Monohydrate
- Manufacturer
- Recordati Netherlands
- Country
- Belgium (BE)
- ATC code
- L01EK03
- ATC class
- Tivozanib
- Defined daily dose
- 1 mg, O
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 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
7 interactions on record for tivozanib.
Graded by severity as the source publishes them — 3 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
Tivozanib · interactions on record
7 records
- 3 severe
- 4 moderate
Most severe, free to view
- PhenobarbitalN03AA02severe
- PhenobarbitalN05CA24severe
- Hyperici herbaN06AX25severe
- RiociguatC02KX05moderate
- 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
Tivozanib in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesFOTIVDAAVEO Pharmaceuticals, Inc.
- SpainFOTIVDA 890 MICROGRAMOS CAPSULAS DURASRecordati Netherlands B.V.
- FinlandFotivdaRecordati Netherlands B.V.
- United KingdomFotivda 890microgram capsulesRecordati UK Ltd
- IrelandFotivda 890 microgram hard capsulesEUSA Pharma (Netherlands) B.V.
- CzechiaFOTIVDARecordati Netherlands B.V., Schiphol-Rijk
- NorwayFotivdaRecordati Netherlands B.V.
- PolandFotivdaEUSA Pharma (Netherlands) B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Fotivda
- Liechtenstein · Fotivda
- Norway · Fotivda
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 FAMHP / AFMPS (Belgium). 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/8d0ad497-4968-486f-9e61-45a72268525e GET /v1/drugs/8d0ad497-4968-486f-9e61-45a72268525e?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": "Capsule, hard",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Fotivda 890 µg",
"name_fr": "Fotivda 890 µg",
"name_nl": "Fotivda 890 µg",
"amp_code": "SAM526702-00",
"strengths": [
"890.0000",
"890.0000"
],
"pack_count": 1,
"substances": [
"Tivozanib Hydrochloride Monohydrate",
"Tivozanib",
"E 102",
"Mannitol",
"Propylene Glycol"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Tivozanib",
"authorisation_numbers": [
"EU/1/17/1215/001"
]
}See everything about tivozanib.
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.