United Kingdom· GB-APID-13024811000001103
Phenylpropanolamine 25mg/5ml oral solution
A phenylpropanolamine product containing phenylpropanolamine, registered in United Kingdom by Special Order. The same ATC class is registered in 3 of our 19 countries.
Checked against NHS dm+d (United Kingdom) 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: United Kingdom, from NHS dm+d (United Kingdom)
- 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
NHS dm+d (United Kingdom)- Active substance
- Phenylpropanolamine
- Manufacturer
- Special Order
- Country
- United Kingdom (GB)
- ATC code
- R01BA01
- ATC class
- Phenylpropanolamine
- Defined daily dose
- 0.1 g, O
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 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.
- FinlandPropalinVetoquinol S.A.
- CanadaPROIN CHEWABLE TABLETSPEGASUS LABORATORIES INC
- SwedenRinexin 50 mg DepottablettViatris AB
- NorwayRinexinViatris AS
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 NHS dm+d (United Kingdom). 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/f5ae76f4-9452-4562-8be9-b705be4373e6 GET /v1/drugs/f5ae76f4-9452-4562-8be9-b705be4373e6?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.
{
"apid": "13024811000001103",
"desc": "Phenylpropanolamine 25mg/5ml oral solution (Special Order)",
"form": "Oral solution",
"vpid": "13040811000001106",
"source": "dmd",
"vtm_id": "777185005",
"strength": "5 mg",
"substance": "Phenylpropanolamine",
"ingredient": "Phenylpropanolamine hydrochloride",
"supplier_code": "8286711000001104"
}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.