United Kingdom· GB-APID-16184411000001107
Vedrop 50mg/ml oral solution
A tocofersolan product containing tocofersolan, registered in United Kingdom by Recordati Rare Diseases UK Ltd. The same ATC class is registered in 11 of our 19 countries.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
Where it is registered
Tocofersolan is registered in 11 of 19 countries.
Countries holding a registration under ATC A11HA08 (tocofersolan), each read from that country’s own register.
- This record: United Kingdom, from NHS dm+d (United Kingdom)
- 7 of them publish a price we can compare per daily dose
Tocofersolan · ATC A11HA08
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Tocofersolan
- Manufacturer
- Recordati Rare Diseases UK Ltd
- Country
- United Kingdom (GB)
- ATC code
- A11HA08
- ATC class
- Tocofersolan
- Defined daily dose
- 0.2 g, O
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 2
- gtin3663502000731
- gtin3663502000717
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Tocofersolan in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaVEDROPRecordati Rare Diseases, Puteaux
- SpainVEDROP 50 MG/ML EN SOLUCION ORALRecordati Rare Diseases
- FinlandVedropRecordati Rare Diseases
- FranceVEDROP 50 mg/ml, solution buvableRECORDATI RARE DISEASES
- IrelandVedrop 50 mg/ml Oral solutionRecordati Rare Diseases
- IcelandVedropRecordati Rare Diseases*
- PolandVedropRecordati Rare Diseases
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/f173025a-2f92-4823-aa58-f4ed120d7448 GET /v1/drugs/f173025a-2f92-4823-aa58-f4ed120d7448?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": "16184411000001107",
"desc": "Vedrop 50mg/ml oral solution (Recordati Rare Diseases UK Ltd)",
"form": "Oral solution",
"vpid": "16197911000001106",
"source": "dmd",
"vtm_id": "16239411000001101",
"strength": "50 mg",
"substance": "Tocofersolan",
"ingredient": "Tocofersolan",
"supplier_code": "3371801000001103"
}See everything about tocofersolan.
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.