Germany· DE-A57-a3c2c7ecb079dbb8
Selen
A medicinal product containing sodium selenite, registered in Germany by Laboratoire Aguettant.
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 Selenite
- Manufacturer
- Laboratoire Aguettant
- 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 selenite in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsSelenase drank 100 µg, drank 50 µg/mlBiosyn Arzneimittel GmbH
- BelgiumAddaven 540 µg/mlFresenius Kabi
- FranceSELENIUM OLIGOSOL 100 microgrammes/2 ml, solution buvable en ampouleLABCATAL
- FinlandSeleeni AguettantLaboratoire Aguettant
- United KingdomAddaven concentrate for solution for infusion 10ml ampoulesFresenius Kabi Ltd
- Japan亜セレン酸ナトリウム藤本製薬
Authorised across Europe · EMA
The same active substance is authorised in 8 EEA countries. Names it is sold under:
- Austria · Selen, Selen Fresenius
- Belgium · Selenium Aguettant
- Bulgaria · Cefasel
- France · Oligosol, Selenium Laboratoire Aguettant
- United Kingdom (Northern Ireland) · Selenium Laboratoire Aguettant
- Greece · Motsalon, Sedynam
- Luxembourg · Oligosol, Selenium Aguettant
- Portugal · Selénio Aguettant
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/48c80373-d501-4908-9e9a-9327d080e5dc GET /v1/drugs/48c80373-d501-4908-9e9a-9327d080e5dc?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 Selenite",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about sodium selenite.
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.