Iceland· IS-EU/1/24/1794/001

EXBLIFEP

A cefepim und beta-lactamase-inhibitor product containing cefepimum inn díhýdróklóríð mónóhýdrat,enmetazobactam, registered in Iceland by ADVANZ PHARMA Limited. The same ATC class is registered in 9 of our 19 countries.

ATC J01DE51

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedEXBLIFEPATCJ01DE51REGISTER NO.IS-EU/1/24/1794/001PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Cefepim und beta-lactamase-inhibitor is registered in 9 of 19 countries.

Countries holding a registration under ATC J01DE51 (cefepim und beta-lactamase-inhibitor), each read from that country’s own register.

  • This record: Iceland, from Icelandic Medicines Agency (Iceland)
  • 6 of them publish a price we can compare per daily dose

Cefepim und beta-lactamase-inhibitor · ATC J01DE51

9 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
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
Cefepimum INN díhýdróklóríð mónóhýdrat,Enmetazobactam
Manufacturer
ADVANZ PHARMA Limited
Country
Iceland (IS)
ATC code
J01DE51
ATC class
Cefepim und Beta-Lactamase-Inhibitor
Defined daily dose
6 g, P
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 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.

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/e322a8db-23cc-4e0a-9434-7723844e2afc
GET /v1/drugs/e322a8db-23cc-4e0a-9434-7723844e2afc?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": "Stofn fyrir innrennslisþykkni, lausn",
  "source": "lyfjastofnun",
  "atc_raw": "J01DE51",
  "marketed": false,
  "strength": "2 g /0,5 g",
  "ma_number": "EU/1/24/1794/001",
  "substance": "Cefepimum INN díhýdróklóríð mónóhýdrat,Enmetazobactam",
  "other_info": null,
  "legal_status": "(R) Lyfseðilsskylt",
  "ma_issued_serial": "45372"
}

See everything about cefepim und beta-lactamase-inhibitor.

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.