Poland· PL-100315864
Revestive
A teduglutide product containing teduglutidum, registered in Poland by Takeda Pharmaceuticals International AG Ireland Branch. The same ATC class is registered in 15 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Teduglutide is registered in 15 of 19 countries.
Countries holding a registration under ATC A16AX08 (teduglutide), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 9 of them publish a price we can compare per daily dose
Teduglutide · ATC A16AX08
15 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Sweden
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
URPL (Poland)- Active substance
- Teduglutidum
- Manufacturer
- Takeda Pharmaceuticals International AG Ireland Branch
- Country
- Poland (PL)
- ATC code
- A16AX08
- ATC class
- Teduglutide
- Defined daily dose
- 5 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05060147025408
- gtin05909991256395
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
18 interactions on record for teduglutide.
Graded by severity as the source publishes them — 2 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
Teduglutide · interactions on record
18 records
- 2 severe
- 16 moderate
Most severe, free to view
- BexaroteneL01XF03severe
- BexarotenL01XX25severe
- ClonazepamN03AE01moderate
- MidazolamN03AE02moderate
- 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
Teduglutide 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
- SpainREVESTIVE 5 MG POLVO Y DISOLVENTE PARA SOLUCION INYECTABLETakeda Pharmaceuticals International Ag Ireland Branch
- IcelandRevestiveTakeda Pharmaceuticals International AG Ireland Branch
- BelgiumRevestive 5 mgTakeda Pharmaceuticals International Ireland Branch
- SwitzerlandRevestive 5 mg, Pulver und Lösungsmittel zur Herstellung einer InjektionslösungTakeda Pharma AG
- NorwayRevestiveTakeda Pharmaceuticals International AG Ireland Branch
- United KingdomRevestive 5mg powder and solvent for solution for injection vialsTakeda UK Ltd
- FinlandRevestiveOrifarm Oy
Authorised across Europe · EMA
The same active substance is authorised in 7 EEA countries. Names it is sold under:
- Austria · Tidonalle
- Spain · Teduglutida Cipla
- 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 URPL (Poland). 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/873fd6d5-7527-4d4d-a9b2-1af7bed083da GET /v1/drugs/873fd6d5-7527-4d4d-a9b2-1af7bed083da?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": "Proszek i rozpuszczalnik do sporządzania roztworu do wstrzykiwań",
"source": "urpl",
"strength": "5 mg",
"packaging": "05909991256395 ¦ Rpz ¦ EU/1/12/787/001 ¦ 91386\n28 fiol. 5 mg proszku ¦ 28 amp.-strzyk. 0,5 ml rozp. + 6 tłoków\n¦ UR/Z/4c/041/26 - 05060147025408\nRpz ¦ EU/1/12/787/002 ¦ 122771\n1 fiol. 5 mg proszku ¦ 1 amp.-strzyk. 0,5 ml rozp.",
"substance": "Teduglutidum 5 mg",
"common_name": "Teduglutidum",
"pl_product_id": "100315864",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about teduglutide.
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.