Poland· PL-100109521

Migea

A tolfenamic acid product containing acidum tolfenamicum, registered in Poland by Sandoz GmbH. The same ATC class is registered in 5 of our 19 countries.

ATC M01AG02

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedMigeaATCM01AG02REGISTER NO.PL-100109521PACKS LISTED2CHECKEDSeptember 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: Poland, from URPL (Poland)
  • 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

URPL (Poland)
Active substance
Acidum tolfenamicum
Manufacturer
Sandoz GmbH
Country
Poland (PL)
ATC code
M01AG02
ATC class
Tolfenamic acid
Defined daily dose
0.3 g, O
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909990954216
  • gtin
    05907626703221

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
  • Finland · Clotam
  • Greece · Gantil
  • Norway · 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 URPL (Poland). 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/f0cf7f38-e588-4b16-8f6d-67e9dac52388
GET /v1/drugs/f0cf7f38-e588-4b16-8f6d-67e9dac52388?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": "Tabletki",
  "source": "urpl",
  "strength": "200 mg",
  "packaging": "05909990954216 ¦ Rp ¦ Skasowane ¦ 19566\n10 tabl.\n05907626703221 ¦ OTC ¦ 106367\n4 tabl.",
  "substance": "Acidum tolfenamicum 200 mg",
  "common_name": "Acidum tolfenamicum",
  "pl_product_id": "100109521",
  "pozwolenie_nr": "09542",
  "auth_procedure": "NAR",
  "authorisation_validity": "Bezterminowe"
}

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.