Czechia· CZ-0231842
BAT [BOTULISM ANTITOXIN HEPTAVALENT (A, B, C, D, E, F, G) (EQUINE)
A botulismus-antitoxin product containing botulinum antitoxin type a + botulinum antitoxin type b + botulinum antitoxin type c + botulinum antitoxin type d + 3 more, registered in Czechia. The same ATC class is registered in 4 of our 19 countries.
Checked against SÚKL (Czech Republic) on
Informational only — not a medical device.
Where it is registered
Botulismus-antitoxin is registered in 4 of 19 countries.
Countries holding a registration under ATC J06AA04 (botulismus-antitoxin), each read from that country’s own register.
- This record: Czechia, from SÚKL (Czech Republic)
- 3 of them publish a price we can compare per daily dose
Botulismus-antitoxin · ATC J06AA04
4 / 19 countries
- Czechiaprice
- Ireland
- Norwayprice
- Polandprice
The record
At a glance
SÚKL (Czech Republic)- Active substance
- BOTULINUM ANTITOXIN TYPE A + BOTULINUM ANTITOXIN TYPE B + BOTULINUM ANTITOXIN TYPE C + BOTULINUM ANTITOXIN TYPE D + 3 more
- Manufacturer
- —
- Country
- Czechia (CZ)
- ATC code
- J06AA04
- ATC class
- Botulismus-Antitoxin
- 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 class
Other records under J06AA04
Botulismus-antitoxin, as other registers publish it.
- PolandAntytoksyna botulinowa A B EWytwórnia Surowic i Szczepionek Biomed Sp. z o.o.
- CzechiaANTYTOKSYNA BOTULINOWA ABE
- CzechiaANTYTOKSYNA BOTULINOWA ABE
- NorwayAntytoksyna botulinowa ABE biomed
- CzechiaBAT [BOTULISM ANTITOXIN HEPTAVALENT (A, B, C, D, E, F, G) (EQUINE)
- IrelandDysport 500 units Powder for solution for injectionIpsen Pharma
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/b4901f99-019f-4a3d-b38e-98ba62962a3d GET /v1/drugs/b4901f99-019f-4a3d-b38e-98ba62962a3d?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": null,
"pack_size": "1X20ML",
"substance": "BOTULINUM ANTITOXIN TYPE A + BOTULINUM ANTITOXIN TYPE B + BOTULINUM ANTITOXIN TYPE C + BOTULINUM ANTITOXIN TYPE D + 3 more",
"cz_kod_sukl": "0231842",
"product_type": "IM",
"substance_codes": "5163,5164,22030,22031,5165,22028,22032",
"registration_state": "F",
"registration_number": null
}See everything about botulismus-antitoxin.
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.