Spain· ES:1252005001
TEDUGLUTIDA VIATRIS 5 MG POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE EFG
A medicinal product containing teduglutida, registered in Spain by Viatris Limited.
Checked against AEMPS CIMA (Spain) on
Informational only — not a medical device.
The record
At a glance
AEMPS CIMA (Spain)- Active substance
- teduglutida
- Manufacturer
- Viatris Limited
- Country
- Spain (ES)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- AEMPS CIMA (Spain)
- Last checked
- August 12, 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
Teduglutida in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwedenNilleto 5 mg Pulver och vätska till injektionsvätska, lösningFresenius Kabi AB
- IcelandRevestiveTakeda Pharmaceuticals International AG Ireland Branch
- BelgiumRevestive 5 mgTakeda Pharmaceuticals International Ireland Branch
- PolandRevestiveTakeda Pharmaceuticals International AG Ireland Branch
- NorwayRevestiveTakeda Pharmaceuticals International AG Ireland Branch
- United KingdomRevestive 5mg powder and solvent for solution for injection vialsTakeda UK Ltd
- SwitzerlandRevestive 5 mg, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungTakeda Pharma AG
- FinlandRevestiveOrifarm Oy
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Austria · Tidonalle
- France · Téduglutide, Teduglutide Adalvo
- Iceland · Revestive, Teduglutide Viatris
- Liechtenstein · Revestive, Teduglutide Viatris
- Norway · Niletto, Revestive
- Sweden · Nilleto, Teduglutid Cipla
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 AEMPS CIMA (Spain). 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/a165dd26-bc37-4391-a901-289afd01e68e GET /v1/drugs/a165dd26-bc37-4391-a901-289afd01e68e?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.
{
"cpresc": "Uso Hospitalario",
"estado": "{\"aut\":1770291905000}",
"nregistro": "1252005001",
"substance": "teduglutida"
}See everything about teduglutida.
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.