Sweden· SE-20181003000014
Pro-Epanutin 75 mg/ml (50 mgFE/ml) Koncentrat till infusionsvätska, lösning/injektionsvätska, lösning
A medicinal product containing fosphenytoin sodium, registered in Sweden by Orifarm AB.
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Fosphenytoin Sodium
- Manufacturer
- Orifarm AB
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer20181003000014
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fosphenytoin sodium in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandPro-EpanutinPfizer Oy
- NorwayPro-EpanutinPfizer AS
- United StatesCEREBYXPfizer Laboratories Div Pfizer Inc
- GermanyFosphenytoin DesitinDesitin Arzneimittel Gmbh
- United KingdomPro-Epanutin 750mg/10ml concentrate for solution for injection vialsPfizer Ltd
- CanadaCEREBYXSEARCHLIGHT PHARMA INC
- IcelandPro-EpanutinPfizer ApS
- IrelandPro-Epanutin 75 mg/ml concentrate for solution for infusion/solution for injectionPfizer Healthcare Ireland Unlimited Company
Authorised across Europe · EMA
The same active substance is authorised in 8 EEA countries. Names it is sold under:
- Germany · Fosphenytoin Desitin
- Denmark · Pro-Epanutin
- Finland · Pro-Epanutin
- France · Fosphenytoine Arrow, Prodilantin
- United Kingdom (Northern Ireland) · Pro-Epanutin
- Ireland · Pro-Epanutin
- Iceland · Pro-Epanutin
- Norway · Pro-Epanutin
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 Swedish Medical Products Agency (Sweden). 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/ff70d485-aa44-478e-873a-6715a4269bae GET /v1/drugs/ff70d485-aa44-478e-873a-6715a4269bae?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.
{
"source": "lakemedelsverket",
"doc_types": [
"PL"
],
"se_npl_id": "20181003000014",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20181003000014",
"product_doc_link": "https://docetp.mpa.se/LMF/Pro-Epanutin%2075%20mg%20per%20ml%20%2850%20mgFE%20per%20ml%29%20concentrate%20for%20solution%20for%20infusion%20or%20solution%20for%20injection%20DK%20PL_09001bee8092778f.pdf"
}See everything about fosphenytoin sodium.
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.