Finland· FI-REL-REL4722

Atrovent

A ipratropium bromide product containing ipratropium bromide, registered in Finland by Paranova Oy. The same ATC class is registered in 13 of our 19 countries.

ATC R03BB01

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedAtroventATCR03BB01REGISTER NO.FI-REL-REL4722PACKS LISTED0CHECKEDSeptember 27, 2026

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: Finland, from Fimea (Finland)
  • 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
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

Fimea (Finland)
Active substance
Ipratropium bromide
Manufacturer
Paranova Oy
Country
Finland (FI)
ATC code
R03BB01
ATC class
Ipratropium bromide
Defined daily dose
0.12 mg, Inhal
Reimbursed
Not published by this register
Source register
Fimea (Finland)
Last checked
September 27, 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.

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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

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.

All ipratropium bromide products

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
  • 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
  • Iceland · Atrovent, Lomuspray
  • 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 Fimea (Finland). 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/17578e6c-479a-4595-b5b9-b1a8d3bd7aa5
GET /v1/drugs/17578e6c-479a-4595-b5b9-b1a8d3bd7aa5?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.

{
  "ddd": "0.12",
  "form": "inhalaatiojauhe",
  "route": null,
  "ddd_unit": "mg",
  "strength": "40 mikrog",
  "atc_label": "ipratropiumbromidi",
  "ma_number": "12492",
  "auth_status": "Myyntilupa peruuntunut",
  "eu_ma_number": null,
  "fimea_rel_id": "REL4722",
  "authorised_at": "1996-09-02"
}

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.