Finland· FI-REL-REL3146
Dimetane Expect.
A antitussiva und expektoranzien product containing guaifenesin + brompheniramine maleate + phenylpropanolamine hydrochloride + phenylephrine hydrochloride, registered in Finland by John Wyeth & Brother Ltd. The same ATC class is registered in 6 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Antitussiva und expektoranzien is registered in 6 of 19 countries.
Countries holding a registration under ATC R05FB02 (antitussiva und expektoranzien), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 5 of them publish a price we can compare per daily dose
Antitussiva und expektoranzien · ATC R05FB02
6 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Finlandprice
- Polandprice
- Switzerlandprice
The record
At a glance
Fimea (Finland)- Active substance
- Guaifenesin + Brompheniramine maleate + Phenylpropanolamine hydrochloride + Phenylephrine hydrochloride
- Manufacturer
- John Wyeth & Brother Ltd
- Country
- Finland (FI)
- ATC code
- R05FB02
- ATC class
- Antitussiva und Expektoranzien
- 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.
Same class
Other records under R05FB02
Antitussiva und expektoranzien, as other registers publish it.
- SwitzerlandAmavita BronchialpastillenAmavita Health Care AG
- SwitzerlandCarmol GouttesVerfora SA
- SwitzerlandCarmol GouttesVerfora SA
- SwitzerlandCarmol GouttesVerfora SA
- SwitzerlandCarmol GouttesVerfora SA
- SwitzerlandCarmol GouttesVerfora SA
- SwitzerlandCarmol GouttesVerfora SA
- FinlandCodetabsOrifarm Healthcare A/S
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/3e30227a-fbed-46b0-a5aa-d1f11274d130 GET /v1/drugs/3e30227a-fbed-46b0-a5aa-d1f11274d130?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": "6",
"form": "mikstuura",
"route": null,
"ddd_unit": "ED",
"strength": null,
"atc_label": "yskänhillitsijät ja ekspektorantit, lukuun ottamatta mukolyyttejä",
"ma_number": "10693",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL3146",
"authorised_at": "1992-03-25"
}See everything about antitussiva und expektoranzien.
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.