Iceland· IS-IS/1/12/039/01

Penomax

A pivmecillinam product containing pivmecillinamum inn hýdróklóríð, registered in Iceland by Orion Corporation. The same ATC class is registered in 12 of our 19 countries.

ATC J01CA08

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedPenomaxATCJ01CA08REGISTER NO.IS-IS/1/12/039/01PACKS LISTED3CHECKEDSeptember 29, 2026

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
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

Icelandic Medicines Agency (Iceland)
Active substance
Pivmecillinamum INN hýdróklóríð
Manufacturer
Orion Corporation
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 · 3

3 priced
  • ean
    148263
    20 stk x1 þpakki
    ISK 2777
  • ean
    148274
    30 stk x1 þpakki
    ISK 3835
  • ean
    148285
    100 stk x1 glas
    ISK 9172

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.

All pivmecillinam products

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/d1aaaead-1f69-433b-9c4b-ed432dcd0ea4
GET /v1/drugs/d1aaaead-1f69-433b-9c4b-ed432dcd0ea4?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": "200 mg",
  "ma_number": "IS/1/12/039/01",
  "substance": "Pivmecillinamum INN hýdróklóríð",
  "other_info": null,
  "legal_status": "(R) Lyfseðilsskylt",
  "ma_issued_serial": "41019"
}

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.