Iceland· IS-880161
Atrovent
A ipratropium bromide product containing ipratropii bromidum inn, registered in Iceland by Boehringer Ingelheim International GmbH*. The same ATC class is registered in 13 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Ipratropium bromide is registered in 13 of 19 countries.
Countries holding a registration under ATC R03BB01 (ipratropium bromide), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 8 of them publish a price we can compare per daily dose
Ipratropium bromide · ATC R03BB01
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Ipratropii bromidum INN
- Manufacturer
- Boehringer Ingelheim International GmbH*
- Country
- Iceland (IS)
- ATC code
- R03BB01
- ATC class
- Ipratropium bromide
- Defined daily dose
- 0.12 mg, Inhal
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 1
1 priced- ean12981760 sk-ílát x1 pakkiISK 6443
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
114 interactions on record for ipratropium bromide.
Graded by severity as the source publishes them — 114 moderate. 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
Ipratropium bromide · interactions on record
114 records
- 114 moderate
Most severe, free to view
- DicycloverineA03AA07moderate
- PropanthelineA03AB05moderate
- MepenzolateA03AB12moderate
- TrospiumA03AB20moderate
- 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
Ipratropium bromide in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceIPRATROPIUM AGUETTANT ADULTES 0,5 mg/2 ml, solution pour inhalation par nébuliseur en récipient unidoseAGUETTANT
- SwedenAtrovent 0,25 mg/ml Lösning för nebulisatorBoehringer Ingelheim International GmbH
- BelgiumAtrovent 0.5 mg/2 mlBoehringer Ingelheim
- NetherlandsAtrovent Unit Dose 500 microgram/2 ml, verneveloplossingBoehringer Ingelheim B.V.
- IrelandAtrovent 250 UDVs 250 micrograms/ 1ml Nebuliser SolutionBoehringer Ingelheim International GmbH
- SpainATROVENT MONODOSIS 500 mcg/ 2ml SOLUCION PARA INHALACION POR NEBULIZADORBoehringer Ingelheim Espana S.A.
- NorwayAtroventBoehringer Ingelheim International GmbH
- FinlandAtroventParanova Oy
Authorised across Europe · EMA
The same active substance is authorised in 26 EEA countries. Names it is sold under:
- Austria · Atrovent - Dosieraerosol, Ipratropiumbromid Infectopharm
- Belgium · Atrovent, Atrovent Hfa
- Cyprus · Atrovent
- Czechia · Atrovent, Atrovent N
- Germany · Atrovent, Atrovent Ls
- Denmark · Atrovent, Ipratropiumbromid Teva
- Estonia · Atrovent N
- Spain · Atroaldo, Atrovent
- Finland · Atrovent, Atrovent Eco
- France · Atrovent, Atrovent Adultes
- United Kingdom (Northern Ireland) · Atrovent Inhaler Cfc-Free, Atrovent Udvs
- Greece · Atrovent, Broncovent
- Croatia · Atrovent, Atrovent N
- Hungary · Atrovent N
- Ireland · Atrovent 250 Udvs, Atrovent 500 Udvs
- Italy · Atem, Nasipral
- Lithuania · Atrovent N
- Luxembourg · Atrovent, Atrovent Hfa
- Malta · Atroaldo, Atrovent Inhaler Cfc-Free
- Netherlands · Atrovent, Atrovent Unit Dose
- Norway · Atrovent, Ipraxa
- Poland · Atrodil, Atrovent
- Portugal · Atrovent, Atrovent Pa
- Romania · Ipravent Inhaler
- Sweden · Atrovent, Ipravent
- Slovakia · Atrovent N
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/226cb771-ee6e-4f14-9c22-f7ddb24b34b5 GET /v1/drugs/226cb771-ee6e-4f14-9c22-f7ddb24b34b5?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": "Lausn í eimgjafa",
"source": "lyfjastofnun",
"atc_raw": "R03BB01",
"marketed": true,
"strength": "0,25 mg/ml",
"ma_number": "880161",
"substance": "Ipratropii bromidum INN",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "32599"
}See everything about ipratropium bromide.
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.