Germany· DE-A57-5b6065902b5846cc
Flector
A medicinal product containing diclofenac epolamine, registered in Germany by Ibsa Farmaceutici Italia.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Diclofenac Epolamine
- Manufacturer
- Ibsa Farmaceutici Italia
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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
Diclofenac epolamine in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaFLALGOIBSA Slovakia s.r.o., Bratislava
- United Statesdiclofenac epolamineTeva Pharmaceuticals USA Inc.
- BelgiumDiclofenac IBSA Farmaceutici 140 mgIBSA Farmaceutici Italia
- IrelandDiclofenac 140 mg medicated plasterIBSA Farmaceutici Italia S.r.l
Authorised across Europe · EMA
The same active substance is authorised in 17 EEA countries. Names it is sold under:
- Austria · Flector Ep
- Belgium · Diclofenac Patch Ab, Flalgo
- Cyprus · Flector Tissugel
- Czechia · Flalgo, Flector
- Denmark · Flector
- Spain · Flectormed
- France · Diclofenac Urgo, Flector
- United Kingdom (Northern Ireland) · Dicloalgan, Flector Tissugel
- Greece · Dicloplast, Miniflampatch
- Hungary · Diclofenac Epolamine Cooper, Flector
- Ireland · Diclofenac, Diclofenac Ibsa Farmaceutici Italia
- Italy · Calminemed, Dicloreum
- Luxembourg · Flector Tissugel
- Poland · Diklofenak Viatris, Dolofest
- Portugal · Diclofenac Farmoz, Flector Tissugel
- Sweden · Flector
- Slovakia · Flectopar, Flector
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 EMA Article 57 (European Union). 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/08e72ff2-2edd-436a-a5a3-80b81c70883c GET /v1/drugs/08e72ff2-2edd-436a-a5a3-80b81c70883c?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.
{
"pzn": null,
"route": "Cutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Diclofenac Epolamine",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about diclofenac epolamine.
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.