Ireland· IE-PA-EU/1/21/1600/001
Tecovirimat SIGA 200 mg hard capsules
A tecovirimat product containing tecovirimat monohydrate, registered in Ireland by SIGA Technologies Netherlands B.V.. The same ATC class is registered in 11 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Tecovirimat is registered in 11 of 19 countries.
Countries holding a registration under ATC J05AX24 (tecovirimat), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 7 of them publish a price we can compare per daily dose
Tecovirimat · ATC J05AX24
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Norwayprice
- Polandprice
- Sweden
- United Kingdom
- United Statesprice
The record
At a glance
HPRA (Ireland)- Active substance
- Tecovirimat Monohydrate
- Manufacturer
- SIGA Technologies Netherlands B.V.
- Country
- Ireland (IE)
- ATC code
- J05AX24
- ATC class
- Tecovirimat
- Defined daily dose
- 1.2 g, O
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/21/1600/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Tecovirimat in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumTecovirimat Siga 200 mgSiga Technologies Netherlands
- CzechiaTECOVIRIMAT SIGASIGA Technologies Netherlands B.V., Breda
- FinlandTecovirimat SIGASIGA Technologies Netherlands B.V.
- United KingdomTpoxx 200mg capsulesImported (United States)
- IcelandTecovirimat SIGASiga Technologies Netherlands B.V.
- NetherlandsTecovirimat SIGA 200 mg, harde capsuleSIGA Technologies Netherlands B.V.
- NorwayTecovirimat sigaSIGA
- PolandTecovirimat SIGASIGA Technologies Netherland B.V.
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- United Kingdom (Northern Ireland) · Tecovirimat Siga
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 HPRA (Ireland). 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/60143e24-15fd-4695-99af-391d7a5cc994 GET /v1/drugs/60143e24-15fd-4695-99af-391d7a5cc994?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": "Capsule, hard",
"routes": [
"Oral use"
],
"source": "hpra",
"atc_all": [
"J05AX24"
],
"strength": null,
"pa_number": "EU/1/21/1600/001",
"substances": [
"Tecovirimat Monohydrate"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "06/01/2022",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about tecovirimat.
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.