Iceland· IS-EU/1/09/533/001-003
Vedrop
A tocofersolan product containing tocofersolan, registered in Iceland by Recordati Rare Diseases*. The same ATC class is registered in 11 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) 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: Iceland, from Icelandic Medicines Agency (Iceland)
- 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
Icelandic Medicines Agency (Iceland)- Active substance
- Tocofersolan
- Manufacturer
- Recordati Rare Diseases*
- Country
- Iceland (IS)
- ATC code
- A11HA08
- ATC class
- Tocofersolan
- Defined daily dose
- 0.2 g, O
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 2
2 priced- ean06601320 ml x1 glasISK 17326
- ean12414160 ml x1 glasISK 45713
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
- FinlandVedropRecordati Rare Diseases
- FranceVEDROP 50 mg/ml, solution buvableRECORDATI RARE DISEASES
- IrelandVedrop 50 mg/ml Oral solutionRecordati Rare Diseases
- PolandVedropRecordati Rare Diseases
- SpainVEDROP 50 MG/ML EN SOLUCION ORALRecordati Rare Diseases
- United KingdomVedrop 50mg/ml oral solutionRecordati Rare Diseases UK Ltd
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Icelandic Medicines Agency (Iceland). 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/f7a1df03-c6d2-4692-b1e2-76dcce5afe2e GET /v1/drugs/f7a1df03-c6d2-4692-b1e2-76dcce5afe2e?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.
{
"form": "Mixtúra, lausn",
"source": "lyfjastofnun",
"atc_raw": "A11HA08",
"marketed": true,
"strength": "50 mg/ml",
"ma_number": "EU/1/09/533/001-003",
"substance": "Tocofersolan",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í meltingarsjúkdómum barna.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "40122"
}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.