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Finland· FI-REL-REL25577

Geloplasma

A gelatine product containing gelatin + sodium chloride + magnesium chloride hexahydrate + potassium chloride + 1 more, registered in Finland by Fresenius Kabi AB. The same ATC class is registered in 9 of our 19 countries.

ATC B05AA06

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedGeloplasmaATCB05AA06REGISTER NO.FI-REL-REL25577PACKS LISTED0CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about gelatin + sodium chloride + magnesium chloride hexahydrate + potassium chloride + 1 moreAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Gelatine is registered in 9 of 19 countries.

Countries holding a registration under ATC B05AA06 (gelatine), each read from that country’s own register.

  • This record: Finland, from Fimea (Finland)
  • 6 of them publish a price we can compare per daily dose
Search gelatine products by name

Gelatine · ATC B05AA06

9 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
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
Gelatin + Sodium chloride + Magnesium chloride hexahydrate + Potassium chloride + 1 more
Manufacturer
Fresenius Kabi AB
Country
Finland (FI)
ATC code
B05AA06
ATC class
Gelatine
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 class

Other records under B05AA06

Gelatine, as other registers publish it.

All gelatine products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Netherlands · Geloplasma

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/ea515b73-e7b5-4a3e-8d4a-a4fd3343e83e
GET /v1/drugs/ea515b73-e7b5-4a3e-8d4a-a4fd3343e83e?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": "infuusioneste, liuos",
  "route": "Laskimoon",
  "ddd_unit": null,
  "strength": null,
  "atc_label": "gelatiini-polymeerit",
  "ma_number": "21828",
  "auth_status": "Myyntilupa peruuntunut",
  "eu_ma_number": null,
  "fimea_rel_id": "REL25577",
  "authorised_at": "2006-12-21"
}
API referenceMCP serverPlans

See everything about gelatine.

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.

Try it freeOpen in the console