Finland· FI-REL-REL2337

Clotam

A tolfenamic acid product containing tolfenamic acid, registered in Finland by Hexal A/S. The same ATC class is registered in 5 of our 19 countries.

ATC M01AG02

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedClotamATCM01AG02REGISTER NO.FI-REL-REL2337PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Tolfenamic acid is registered in 5 of 19 countries.

Countries holding a registration under ATC M01AG02 (tolfenamic acid), each read from that country’s own register.

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

Tolfenamic acid · ATC M01AG02

5 / 19 countries

  • Denmark
  • Finlandprice
  • Norwayprice
  • Polandprice
  • United Kingdom
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
Tolfenamic acid
Manufacturer
Hexal A/S
Country
Finland (FI)
ATC code
M01AG02
ATC class
Tolfenamic acid
Defined daily dose
0.3 g, 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

Tolfenamic acid in 4 other countries

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

All tolfenamic acid products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • Denmark · Migea
  • Greece · Gantil
  • Norway · Migea
  • Poland · Migea

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/d185d3e6-550c-43b5-9c64-433443798ebf
GET /v1/drugs/d185d3e6-550c-43b5-9c64-433443798ebf?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": "0.3",
  "form": "kapseli, kova",
  "route": null,
  "ddd_unit": "g",
  "strength": "100 mg",
  "atc_label": "tolfenaamihappo",
  "ma_number": "9757",
  "auth_status": "Myyntilupa peruuntunut",
  "eu_ma_number": null,
  "fimea_rel_id": "REL2337",
  "authorised_at": "1988-09-21"
}

See everything about tolfenamic acid.

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.