Sweden· SE-20180115000066
ELOCTA 6000 IE Pulver och vätska till infusionsvätska, lösning
A medicinal product containing efmoroctocog alfa, registered in Sweden by Swedish Orphan Biovitrum AB (publ).
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
- Efmoroctocog Alfa
- Manufacturer
- Swedish Orphan Biovitrum AB (publ)
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- August 27, 2026
Packs & prices · 1
- se_varunummer20180115000066
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Efmoroctocog alfa in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandEloctaSwedish Orphan Biovitrum AB (publ)
- SpainElocta 1000 UI polvo y disolvente para solucion inyectableSwedish Orphan Biovitrum Ab (Publ)
- BelgiumElocta 1000 IUSwedish Orphan Biovitrum (Publ)
- NetherlandsElocta 1000 IU, poeder en oplosmiddel voor oplossing voor injectieSwedish Orphan Biovitrum AB (publ)
- PolandEloctaSwedish Orphan Biovitrum AB (publ)
- FranceELOCTA 1000 UI, poudre et solvant pour solution injectableSWEDISH ORPHAN BIOVITRUM INTERNATIONAL (SUEDE)
- United KingdomElocta 1,000unit powder and solvent for solution for injection vialsSwedish Orphan Biovitrum Ltd
- IrelandELOCTA 1000 IU powder and solvent for solution for injectionSwedish Orphan Biovitrum AB
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Elocta
- Liechtenstein · Elocta
- Norway · Elocta
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/2ca860a9-4b0d-4edc-b5f3-5cd5f82d5d6a GET /v1/drugs/2ca860a9-4b0d-4edc-b5f3-5cd5f82d5d6a?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": [
"EMA",
"EPAR"
],
"se_npl_id": "20180115000066",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20180115000066",
"product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/elocta"
}See everything about efmoroctocog alfa.
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.