Iceland· IS-IS/1/11/075/01
Selexid
A pivmecillinam product containing pivmecillinamum inn hýdróklóríð, registered in Iceland by Karo Pharma AB*. The same ATC class is registered in 12 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Pivmecillinam is registered in 12 of 19 countries.
Countries holding a registration under ATC J01CA08 (pivmecillinam), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 7 of them publish a price we can compare per daily dose
Pivmecillinam · ATC J01CA08
12 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Germany
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Pivmecillinamum INN hýdróklóríð
- Manufacturer
- Karo Pharma AB*
- Country
- Iceland (IS)
- ATC code
- J01CA08
- ATC class
- Pivmecillinam
- Defined daily dose
- 0.6 g, O
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 2
2 priced- ean05432115 stk x1 þpakkiISK 4138
- ean05433220 stk x1 þpakkiISK 5232
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pivmecillinam in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsSelexid 400 mg filmomhulde tablettenEureco-Pharma B.V.
- SpainSELEXID 400 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFGKaro Pharma Ab
- NorwaySelexidKaro Pharma AB (1)
- PolandX-SystoKaro Pharma AB
- United KingdomPivmecillinam 200mg tabletsMilpharm Ltd
- FinlandSelexidLeo Pharma A/S
- FranceSELEXID 200 mg, comprimé pelliculéKARO PHARMA (SUEDE)
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- Portugal · Selexid
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 Icelandic Medicines Agency (Iceland). 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/f1562493-9e3d-4cc6-9851-10c0173fa4c3 GET /v1/drugs/f1562493-9e3d-4cc6-9851-10c0173fa4c3?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": "Filmuhúðuð tafla",
"source": "lyfjastofnun",
"atc_raw": "J01CA08",
"marketed": true,
"strength": "400 mg",
"ma_number": "IS/1/11/075/01",
"substance": "Pivmecillinamum INN hýdróklóríð",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt",
"ma_issued_serial": "40773"
}See everything about pivmecillinam.
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.