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Germany· DE-A57-2851646c79069be3

Natriumedetat Smartpractice Europe

A sodium edetate product containing sodium edetate, registered in Germany by Smartpractice Europe Gmbh. The same ATC class is registered in 2 of our 19 countries.

ATC S01XA05

Checked against EMA Article 57 (European Union) on

Informational only — not a medical device.

SOURCE REGISTER · DEEMA Article 57 (European Union)normalisedNatriumedetat Smartpractice EuropeATCS01XA05REGISTER NO.DE-A57-2851646c79069b…PACKS LISTED0CHECKEDSeptember 30, 2026

Where it is registered

Sodium edetate is registered in 2 of 19 countries.

Countries holding a registration under ATC S01XA05 (sodium edetate), each read from that country’s own register.

  • This record: Germany, from EMA Article 57 (European Union)
  • 1 of them publish a price we can compare per daily dose

Sodium edetate · ATC S01XA05

2 / 19 countries

  • Germany
  • Norwayprice
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

EMA Article 57 (European Union)
Active substance
Sodium Edetate
Manufacturer
Smartpractice Europe Gmbh
Country
Germany (DE)
ATC code
S01XA05
ATC class
Sodium edetate
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

Sodium edetate in 2 other countries

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

All sodium edetate products

Authorised across Europe · EMA

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

  • France · Chelatran

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/b0f250fb-70bf-449b-be16-3bfc4a09ae93
GET /v1/drugs/b0f250fb-70bf-449b-be16-3bfc4a09ae93?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": "Sodium Edetate",
  "atc_from_source": null,
  "authorisation_country": "Germany"
}

See everything about sodium edetate.

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.