France· FR:61001565
ITOVEBI 3 mg, comprimé pelliculé
A inavolisib product containing inavolisib, registered in France by ROCHE REGISTRATION (ALLEMAGNE). The same ATC class is registered in 10 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
Where it is registered
Inavolisib is registered in 10 of 19 countries.
Countries holding a registration under ATC L01EM06 (inavolisib), each read from that country’s own register.
- This record: France, from Base de données publique des médicaments — BDPM (France)
- 7 of them publish a price we can compare per daily dose
Inavolisib · ATC L01EM06
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- INAVOLISIB
- Manufacturer
- ROCHE REGISTRATION (ALLEMAGNE)
- Country
- France (FR)
- ATC code
- L01EM06
- ATC class
- Inavolisib
- Defined daily dose
- 9 mg, O
- Reimbursed
- No
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
- cip133400930320983plaquette(s) aluminium de 28 comprimé(s)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Inavolisib in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumItovebi 3 mgRoche Registration
- SwitzerlandItovebi 3 mg, FilmtablettenRoche Pharma (Schweiz) AG
- CzechiaITOVEBIRoche Registration GmbH, Grenzach-Wyhlen
- SpainITOVEBI 3 MG COMPRIMIDOS RECUBIERTOS CON PELICULARoche Registration Gmbh
- FinlandItovebiRoche Registration GmbH
- IrelandItovebi 3 mg film-coated tabletsRoche Registration GmbH
- IcelandItovebiRoche Registration GmbH*
- NetherlandsItovebi 3 mg filmomhulde tablettenRoche Registration GmbH
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Itovebi
- Liechtenstein · Itovebi
- Norway · Itovebi
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 Base de données publique des médicaments — BDPM (France). 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/2cff2f5e-3edf-42fe-a6b8-78735592972a GET /v1/drugs/2cff2f5e-3edf-42fe-a6b8-78735592972a?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.
{
"cis": "61001565",
"date_amm": "2025-07-18",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/25/1942",
"substance": "INAVOLISIB",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "comprimé pelliculé",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Oui"
}See everything about inavolisib.
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.