Germany· DE-A57-e820255793d16e0f
Technescan Hdp
A medicinal product containing sodium oxidronate, registered in Germany by Curium Netherlands B.V..
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Sodium Oxidronate
- Manufacturer
- Curium Netherlands B.V.
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sodium oxidronate in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandOsteocisCIS bio international
- United KingdomOsteocis 3mg kit for radiopharmaceutical preparationCurium Pharma UK Ltd
- IrelandTechneScan HDP 3mg, kit for radiopharmaceutical preparationCurium Netherlands B.V.
- SwedenTechneScan HDP 3 mg Beredningssats för radioaktivt läkemedelCurium Netherlands B.V.
- United StatesTechnescan HDPCurium US LLC
Authorised across Europe · EMA
The same active substance is authorised in 17 EEA countries. Names it is sold under:
- Austria · Technescan Hdp
- Belgium · Technescan Hdp
- Czechia · Technescan Hdp
- Denmark · Technescan Hdp
- Spain · Hdp Technescan
- Finland · Technescan Hdp
- France · Osteocis, Technescan Hdp
- United Kingdom (Northern Ireland) · Technescan Hdp
- Hungary · Technescan Hdp
- Ireland · Technescan Hdp
- Italy · Osteocis, Technescan Hdp
- Netherlands · Technescan Hdp
- Norway · Technescan Hdp
- Portugal · Technescan Hdp
- Romania · Technescan Hdp
- Sweden · Technescan Hdp
- Slovakia · Technescan Hdp
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 EMA Article 57 (European Union). 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/35f84b33-200c-494e-83ce-b2c79ef58dc5 GET /v1/drugs/35f84b33-200c-494e-83ce-b2c79ef58dc5?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.
{
"pzn": null,
"route": "Intravenous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Sodium Oxidronate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about sodium oxidronate.
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.