Iceland· IS-IS/1/15/044/01
Spiolto Respimat
A olodaterol und tiotropium bromid product containing tiotropii bromidum inn,olodaterolum inn hýdróklóríð, registered in Iceland by Boehringer Ingelheim International 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
Olodaterol und tiotropium bromid is registered in 10 of 19 countries.
Countries holding a registration under ATC R03AL06 (olodaterol und tiotropium bromid), 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
Olodaterol und tiotropium bromid · ATC R03AL06
10 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Tiotropii bromidum INN,Olodaterolum INN hýdróklóríð
- Manufacturer
- Boehringer Ingelheim International GmbH*
- Country
- Iceland (IS)
- ATC code
- R03AL06
- ATC class
- Olodaterol und Tiotropium bromid
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 4
4 priced- ean43722130 skammtar x1 rörlykISK 9736
- ean49082330 skammtar x3 rörlykISK 24883
- ean56174530 skammtar x1 rörlykISK 9901
- ean57949130 skammtar x3 rörlykISK 25615
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Olodaterol und tiotropium bromid in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaSPIOLTO RESPIMATBoehringer Ingelheim International GmbH, Ingelheim am Rhein
- IrelandSpiolto Respimat 2.5 microgram/2.5 microgram, inhalation solutionPCO Manufacturing Ltd.
- SpainSPIOLTO RESPIMAT 2,5 MICROGRAMOS / 2,5 MICROGRAMOS SOLUCION PARA INHALACIONBoehringer Ingelheim International Gmbh
- United KingdomSpiolto Respimat 2.5micrograms/dose / 2.5micrograms/dose inhalation solution cartridge with deviceBoehringer Ingelheim Ltd
- NetherlandsSpiolto Respimat 2,5 microgram/2,5 microgram, inhalatieoplossingEuro Registratie Collectief B.V.
- FinlandInspiolto RespimatBoehringer Ingelheim International GmbH
- PolandSpiolto RespimatBoehringer Ingelheim International GmbH
- GermanySpiolto RespimatBoehringer Ingelheim International Gmbh
Authorised across Europe · EMA
The same active substance is authorised in 30 EEA countries. Names it is sold under:
- Austria · Spiolto Respimat, Yanimo Respimat
- Belgium · Spiolto Respimat, Yanimo Respimat
- Bulgaria · Спиолто Респимат, Янимо Респимат
- Cyprus · Spiolto Respimat, Yanimo Respimat
- Czechia · Spiolto Respimat
- Germany · Spiolto Respimat, Yanimo Respimat
- Denmark · Spiolto Respimat
- Estonia · Spiolto Respimat
- Spain · Spiolto Respimat, Yanimo Respimat
- Finland · Inspiolto Respimat, Yanimo Respimat
- France · Spiolto Respimat
- United Kingdom (Northern Ireland) · Spiolto Respimat
- Greece · Spiolto Respimat, Yanimo Respimat
- Croatia · Spiolto Respimat
- Hungary · Spiolto Respimat
- Ireland · Spiolto Respimat
- Italy · Spiolto Respimat
- Liechtenstein · Spiolto Respimat, Yanimo Respimat
- Lithuania · Spiolto Respimat
- Luxembourg · Spiolto Respimat, Yanimo Respimat
- Latvia · Spiolto Respimat
- Malta · Spiolto Respimat
- Netherlands · Spiolto Respimat, Yanimo Respimat
- Norway · Spiolto Respimat
- Poland · Spiolto Respimat, Yanimo Respimat
- Portugal · Spiolto Respimat, Yanimo Respimat
- Romania · Spiolto Respimat
- Sweden · Spiolto Respimat, Yanimo Respimat
- Slovenia · Spiolto Respimat
- Slovakia · Spiolto Respimat
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/fe75f57b-aa6e-4135-b068-6c9e59134f88 GET /v1/drugs/fe75f57b-aa6e-4135-b068-6c9e59134f88?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": "Innöndunarlausn",
"source": "lyfjastofnun",
"atc_raw": "R03AL06",
"marketed": true,
"strength": "2,5/2,5 míkróg",
"ma_number": "IS/1/15/044/01",
"substance": "Tiotropii bromidum INN,Olodaterolum INN hýdróklóríð",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "42177"
}See everything about olodaterol und tiotropium bromid.
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.