Finland· FI-REL-REL1186
Rinexin
A phenylpropanolamine product containing phenylpropanolamine hydrochloride, registered in Finland by Viatris Oy. The same ATC class is registered in 3 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Phenylpropanolamine is registered in 3 of 19 countries.
Countries holding a registration under ATC R01BA01 (phenylpropanolamine), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 2 of them publish a price we can compare per daily dose
Phenylpropanolamine · ATC R01BA01
3 / 19 countries
- Finlandprice
- Norwayprice
- United Kingdom
The record
At a glance
Fimea (Finland)- Active substance
- Phenylpropanolamine hydrochloride
- Manufacturer
- Viatris Oy
- Country
- Finland (FI)
- ATC code
- R01BA01
- ATC class
- Phenylpropanolamine
- Defined daily dose
- 0.1 g, 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
Phenylpropanolamine in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwedenRinexin 50 mg DepottablettOrifarm AB
- NorwayRinexinViatris AS
- CanadaPROIN CHEWABLE TABLETSPEGASUS LABORATORIES INC
- United KingdomPhenylpropanolamine 25mg/5ml oral solutionSpecial Order
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Norway · Rinexin
- Sweden · Rinexin
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/6c0a406b-d60a-42d4-bf2d-fd4738523f1c GET /v1/drugs/6c0a406b-d60a-42d4-bf2d-fd4738523f1c?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": "0.1",
"form": "depottabletti",
"route": "Suun kautta",
"ddd_unit": "g",
"strength": "50 mg",
"atc_label": "fenyylipropanoliamiini",
"ma_number": "7517",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL1186",
"authorised_at": "1977-12-14"
}See everything about phenylpropanolamine.
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.