Finland· FI-REL-REL920
Tuxi
A pholcodine product containing pholcodine, registered in Finland by Oy Leiras Finland Ab. The same ATC class is registered in 4 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Pholcodine is registered in 4 of 19 countries.
Countries holding a registration under ATC R05DA08 (pholcodine), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 3 of them publish a price we can compare per daily dose
Pholcodine · ATC R05DA08
4 / 19 countries
- Belgiumprice
- Finlandprice
- Franceprice
- United Kingdom
The record
At a glance
Fimea (Finland)- Active substance
- Pholcodine
- Manufacturer
- Oy Leiras Finland Ab
- Country
- Finland (FI)
- ATC code
- R05DA08
- ATC class
- Pholcodine
- Defined daily dose
- 50 mg, O
- 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 medicine, other countries
Pholcodine in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomBenylin Children's Dry Coughs 2mg/5ml oral solutionMcNeil Products Ltd
- BelgiumBroncho-Pectoralis Pholcodine 15 mg - 300 mgMedgenix Benelux
- FranceBIOCALYPTOL 6,55 mg/5 ml SANS SUCRE, sirop édulcoré à la saccharine sodique et au maltitol liquideZAMBON FRANCE
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Cofsed Paediatric, Galenphol
- Ireland · Pholcodine Wockhardt Uk
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/0208a9c1-6742-498e-8e14-82f31dcc2182 GET /v1/drugs/0208a9c1-6742-498e-8e14-82f31dcc2182?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": "50",
"form": "oraalineste",
"route": null,
"ddd_unit": "mg",
"strength": null,
"atc_label": "folkodiini",
"ma_number": "6677",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL920",
"authorised_at": "1973-11-14"
}See everything about pholcodine.
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.