Poland· PL-100009713
Berotec N 100
A fenoterol product containing fenoteroli hydrobromidum, registered in Poland by Boehringer Ingelheim International GmbH. The same ATC class is registered in 3 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Fenoterol is registered in 3 of 19 countries.
Countries holding a registration under ATC R03AC04 (fenoterol), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 3 of them publish a price we can compare per daily dose
Fenoterol · ATC R03AC04
3 / 19 countries
- Finlandprice
- Norwayprice
- Polandprice
The record
At a glance
URPL (Poland)- Active substance
- Fenoteroli hydrobromidum
- Manufacturer
- Boehringer Ingelheim International GmbH
- Country
- Poland (PL)
- ATC code
- R03AC04
- ATC class
- Fenoterol
- Defined daily dose
- 0.6 mg, Inhal
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
1 priced- gtin059099903764141 poj.po 10 ml (200 daw.)PLN 24.1
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fenoterol in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandBerotecBoehringer Ingelheim International GmbH
- GermanyBerotec N Dosier-AerosolBoehringer Ingelheim Pharma Gmbh & Co. Kg
- Japanフェノテロール臭化水素酸塩日本ベーリンガーインゲルハイム
- United KingdomBerotec 200micrograms/dose inhalerBoehringer Ingelheim Ltd
- NorwayBerotec NBoehringer Ingelheim
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Germany · Berotec N Dosier-Aerosol, Partusisten
- Estonia · Berotec N
- Lithuania · Berotec 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 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/79f3d76b-5680-44d1-a661-4d855bb0c442 GET /v1/drugs/79f3d76b-5680-44d1-a661-4d855bb0c442?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": "Aerozol inhalacyjny, roztwór",
"source": "urpl",
"strength": "100 mcg/dawkę inh.",
"packaging": "05909990376414 ¦ Rp ¦ 1831\n1 poj. 10 ml (200 dawek)",
"substance": "Fenoteroli hydrobromidum 100 mcg",
"common_name": "Fenoteroli hydrobromidum",
"pl_product_id": "100009713",
"pozwolenie_nr": "03764",
"auth_procedure": "NAR",
"authorisation_validity": "Bezterminowe"
}See everything about fenoterol.
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.