Iceland· IS-EU/1/00/165/008

Ovitrelle

A choriogonadotropin alfa product containing choriongonadotropinum alfa inn, registered in Iceland by Merck Europe B.V.*. The same ATC class is registered in 14 of our 19 countries.

ATC G03GA08

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedOvitrelleATCG03GA08REGISTER NO.IS-EU/1/00/165/008PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Choriogonadotropin alfa is registered in 14 of 19 countries.

Countries holding a registration under ATC G03GA08 (choriogonadotropin alfa), each read from that country’s own register.

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

Choriogonadotropin alfa · ATC G03GA08

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Italyprice
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • 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
Choriongonadotropinum alfa INN
Manufacturer
Merck Europe B.V.*
Country
Iceland (IS)
ATC code
G03GA08
ATC class
Choriogonadotropin alfa
Defined daily dose
0.25 mg, 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/edc3f694-7859-4c00-b8fa-2b0ccd416d05
GET /v1/drugs/edc3f694-7859-4c00-b8fa-2b0ccd416d05?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": "Stungulyf, lausn í áfylltum lyfjapenna",
  "source": "lyfjastofnun",
  "atc_raw": "G03GA08",
  "marketed": true,
  "strength": "250 míkróg",
  "ma_number": "EU/1/00/165/008",
  "substance": "Choriongonadotropinum alfa INN",
  "other_info": "Ávísun lyfsins er bundin við sérfræðinga í kvensjúkdómum og fæðingahjálp, sérfræðinga í þvagfæraskurðlækningum og við sérfræðinga í innkirtlasjúkdómum.",
  "legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
  "ma_issued_serial": "40717"
}

See everything about choriogonadotropin alfa.

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.