United Kingdom· GB-APID-38700611000001100
Adynovi 2,000unit powder and solvent for solution for injection vials
A rurioctocog alfa pegol product containing rurioctocog alfa pegol, registered in United Kingdom by Takeda UK Ltd. The same ATC class is registered in 2 of our 19 countries.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
Where it is registered
Rurioctocog alfa pegol is registered in 2 of 19 countries.
Countries holding a registration under ATC B02BD38 (rurioctocog alfa pegol), each read from that country’s own register.
- This record: United Kingdom, from NHS dm+d (United Kingdom)
- 1 of them publish a price we can compare per daily dose
Rurioctocog alfa pegol · ATC B02BD38
2 / 19 countries
- Italyprice
- United Kingdom
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Rurioctocog alfa pegol
- Manufacturer
- Takeda UK Ltd
- Country
- United Kingdom (GB)
- ATC code
- B02BD38
- ATC class
- Rurioctocog alfa pegol
- Defined daily dose
- 1 TSD, E
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 2
- gtin00642621076431
- gtin00642621069129
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Rurioctocog alfa pegol in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandAdynovi
- CzechiaADYNOVIBaxalta Innovations GmbH, Vídeň
- BelgiumAdynovi 1000 IU/2 mlBaxalta Innovations
- SwedenADYNOVI 1000 IE/2 ml Pulver och vätska till injektionsvätska, lösningBaxalta Innovations GmbH
- FinlandAdynoviBaxalta Innovations GmbH
- IcelandAdynoviBaxalta Innovations GmbH
- NetherlandsAdynovi 1000 IE/2 ml, poeder en oplosmiddel voor oplossing voor injectieBaxalta Innovations GmbH
- Japanルリオクトコグ アルファ ペゴル（遺伝子組換え）武田薬品工業
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Adynovi
- Liechtenstein · Adynovi
- Norway · Adynovi
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/ff6512a2-4fa9-4258-a1aa-2525c4f6fa5c GET /v1/drugs/ff6512a2-4fa9-4258-a1aa-2525c4f6fa5c?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": "38700611000001100",
"desc": "Adynovi 2,000unit powder and solvent for solution for injection vials (Takeda UK Ltd)",
"form": "Powder and solvent for solution for injection",
"vpid": "38703611000001109",
"source": "dmd",
"vtm_id": "38702711000001108",
"strength": "2000 unit",
"substance": "Rurioctocog alfa pegol",
"ingredient": "Rurioctocog alfa pegol",
"supplier_code": "3811601000001107"
}See everything about rurioctocog alfa pegol.
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.