Finland· FI-REL-REL1805

Receptal vet

A busereliini product containing buserelin acetate, registered in Finland by Intervet International B.V.. The same ATC class is registered in 2 of our 19 countries.

ATC QH01CA90

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedReceptal vetATCQH01CA90REGISTER NO.FI-REL-REL1805PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Buserelin acetate is registered in 2 of 19 countries.

Countries holding a registration under ATC QH01CA90 (busereliini), each read from that country’s own register.

  • This record: Finland, from Fimea (Finland)
  • 1 of them publish a price we can compare per daily dose

Buserelin acetate · ATC QH01CA90

2 / 19 countries

  • Denmark
  • Finlandprice
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

Fimea (Finland)
Active substance
Buserelin acetate
Manufacturer
Intervet International B.V.
Country
Finland (FI)
ATC code
QH01CA90
ATC class
Busereliini
Reimbursed
Not published by this register
Source register
Fimea (Finland)
Last checked
September 27, 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.

Same medicine, other countries

Buserelin acetate in 10 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All buserelin acetate products

Authorised across Europe · EMA

The same active substance is authorised in 10 EEA countries. Names it is sold under:

  • Austria · Suprecur, Suprefact
  • Bulgaria · Супрефакт Депо 3 Месеца
  • Germany · Profact Depot, Profact Pro Injectione
  • Spain · Suprefact, Suprefact Depot
  • United Kingdom (Northern Ireland) · Buserelin, Suprecur Injection
  • Greece · Suprefact Depot 3 Μήνεσ
  • Hungary · Suprefact
  • Italy · Suprefact, Suprefact Depot
  • Netherlands · Suprefact Depot
  • Sweden · Suprecur, Suprefact

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 Fimea (Finland). 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/fba9e63f-823a-4db3-a192-5b84bbdd35e7
GET /v1/drugs/fba9e63f-823a-4db3-a192-5b84bbdd35e7?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.

{
  "ddd": null,
  "form": "injektioneste, liuos",
  "route": "Ihon alle",
  "ddd_unit": null,
  "strength": "4 mikrog/ml",
  "atc_label": "Busereliini",
  "ma_number": "8945",
  "auth_status": "Myyntilupa myönnetty",
  "eu_ma_number": null,
  "fimea_rel_id": "REL1805",
  "authorised_at": "1985-01-23"
}

See everything about buserelin acetate.

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.