Poland· PL-100520929

Sephience

A various alimentary tract and metabolism products product containing sepiapterinum, registered in Poland by PTC Therapeutics International Ltd.. The same ATC class is registered in 4 of our 19 countries.

ATC A16AX

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedSephienceATCA16AXREGISTER NO.PL-100520929PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Sepiapterinum is registered in 4 of 19 countries.

Countries holding a registration under ATC A16AX (various alimentary tract and metabolism products), 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

Sepiapterinum · ATC A16AX

4 / 19 countries

  • Finlandprice
  • Ireland
  • Polandprice
  • Switzerlandprice
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
Sepiapterinum
Manufacturer
PTC Therapeutics International Ltd.
Country
Poland (PL)
ATC code
A16AX
ATC class
Various alimentary tract and metabolism products
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    03400930318881

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Sepiapterinum in 11 other countries

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

All sepiapterinum products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Sephience
  • Liechtenstein · Sephience
  • Norway · Sephience

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/98e1371a-26b8-4804-b885-a32c8ccead75
GET /v1/drugs/98e1371a-26b8-4804-b885-a32c8ccead75?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": "Proszek doustny w saszetce",
  "source": "urpl",
  "strength": "250 mg",
  "packaging": "03400930318881 ¦ Rpz ¦ EU/1/25/1939/001 ¦ 162763\n30 saszetek",
  "substance": "Sepiapterinum 250 mg",
  "common_name": "Sepiapterinum",
  "pl_product_id": "100520929",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about sepiapterinum.

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.