Finland· FI-REL-REL41199

Nuedexta

A dextromethorphan, kombinationen product containing dextromethorphan hydrobromide + quinidine, registered in Finland by Jenson Pharmaceutical Services Ltd.. The same ATC class is registered in 4 of our 19 countries.

ATC N07XX59

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedNuedextaATCN07XX59REGISTER NO.FI-REL-REL41199PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Dextromethorphan, kombinationen is registered in 4 of 19 countries.

Countries holding a registration under ATC N07XX59 (dextromethorphan, kombinationen), each read from that country’s own register.

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

Dextromethorphan, kombinationen · ATC N07XX59

4 / 19 countries

  • Belgiumprice
  • Finlandprice
  • Norwayprice
  • 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

Fimea (Finland)
Active substance
Dextromethorphan hydrobromide + Quinidine
Manufacturer
Jenson Pharmaceutical Services Ltd.
Country
Finland (FI)
ATC code
N07XX59
ATC class
Dextromethorphan, Kombinationen
Defined daily dose
40 mg, O
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

Dextromethorphan, kombinationen in 1 other country

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

All dextromethorphan, kombinationen products

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/43f38b77-3c22-41cf-b85e-c519ab2acd6c
GET /v1/drugs/43f38b77-3c22-41cf-b85e-c519ab2acd6c?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": "40",
  "form": "kapseli, kova",
  "route": null,
  "ddd_unit": "mg",
  "strength": "23 mg / 9 mg",
  "atc_label": "dekstrometorfaani, yhdistelmävalmisteet",
  "ma_number": null,
  "auth_status": "Myyntilupa peruuntunut",
  "eu_ma_number": "EU/1/13/833/003",
  "fimea_rel_id": "REL41199",
  "authorised_at": "2013-06-24"
}

See everything about dextromethorphan, kombinationen.

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.