Czechia· CZ-0018760
SELENASE INJEKČNÍ ROZTOK 500 MCG
A sodium selenite product containing sodium selenite pentahydrate, registered in Czechia by biosyn Arzneimittel GmbH, Fellbach. The same ATC class is registered in 2 of our 19 countries.
Checked against SÚKL (Czech Republic) on
Informational only — not a medical device.
Where it is registered
Sodium selenite is registered in 2 of 19 countries.
Countries holding a registration under ATC B05XA20 (sodium selenite), each read from that country’s own register.
- This record: Czechia, from SÚKL (Czech Republic)
- 1 of them publish a price we can compare per daily dose
Sodium selenite · ATC B05XA20
2 / 19 countries
- Czechiaprice
- Denmark
The record
At a glance
SÚKL (Czech Republic)- Active substance
- SODIUM SELENITE PENTAHYDRATE
- Manufacturer
- biosyn Arzneimittel GmbH, Fellbach
- Country
- Czechia (CZ)
- ATC code
- B05XA20
- ATC class
- Sodium selenite
- Defined daily dose
- 0.2 mg, P
- Reimbursed
- Not published by this register
- Source register
- SÚKL (Czech Republic)
- Last checked
- September 28, 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 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwedenSelesyn 50 mikrogram/ml Injektionsvätska, lösningbiosyn Arzneimittel GmbH
- GermanyCefaselCefak Kg
- IrelandSelesyn 100 micrograms/2 ml, oral solution (50 micrograms/ml)biosyn Arzneimittel GmbH
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Selenase
- Germany · Cefasel, Selen-Loges
- Denmark · Selesyn
- France · Selenium Panpharma
- United Kingdom (Northern Ireland) · Selenase
- Hungary · Selesyn
- Ireland · Selesyn
- Italy · Selesyn
- Luxembourg · Selenase Peroral, Selenase Pro Injectione
- Netherlands · Selenase
- Portugal · Selenase
- Sweden · Selesyn
- Slovakia · Selenase
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 SÚKL (Czech Republic). 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/0294d9af-840c-47ee-a4f2-684709c1e44b GET /v1/drugs/0294d9af-840c-47ee-a4f2-684709c1e44b?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.
{
"form": "INJ SOL",
"source": "sukl",
"strength": "50MCG/ML",
"pack_size": "2X10ML",
"substance": "SODIUM SELENITE PENTAHYDRATE",
"cz_kod_sukl": "0018760",
"product_type": "CH",
"substance_codes": "5637",
"registration_state": "R",
"registration_number": "91/590/05-C"
}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.