Poland· PL-100187018

Ladybon

A g03dc05 product containing tibolonum, registered in Poland by Zentiva, k.s..

ATC G03DC05

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedLadybonATCG03DC05REGISTER NO.PL-100187018PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

URPL (Poland)
Active substance
Tibolonum
Manufacturer
Zentiva, k.s.
Country
Poland (PL)
ATC code
G03DC05
ATC class
G03DC05
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909990668854
  • gtin
    05909990668861

Regulatory notes

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

Same medicine, other countries

G03dc05 in 15 other countries

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

All g03dc05 products

Authorised across Europe · EMA

The same active substance is authorised in 25 EEA countries. Names it is sold under:

  • Austria · Liviel, Tiloria
  • Belgium · Heria, Livial
  • Bulgaria · Айвиал, Ливиал
  • Cyprus · Livial
  • Czechia · Ladybon, Livial
  • Germany · Liviella, Tibolon Aristo
  • Denmark · Livial, Tibocina
  • Spain · Boltin, Tibicare
  • Finland · Livial, Tibocina
  • France · Livial, Tibolone Ccd
  • United Kingdom (Northern Ireland) · Livial, Tibolone Aristo Pharma Gmbh
  • Greece · Juliette, Livial
  • Hungary · Ladybon, Livial
  • Ireland · Livial, Tibolone Aristo
  • Iceland · Livial
  • Italy · Livial, Menec
  • Lithuania · Livial
  • Luxembourg · Heria, Livial
  • Netherlands · Livial, Tibolinia
  • Norway · Livial, Tibocina
  • Portugal · Clitax, Goldar
  • Romania · Livial
  • Sweden · Livial, Tibelia
  • Slovenia · Livial
  • Slovakia · Ladybon, Livial

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/abe61f77-b4fc-4f17-ab10-7bf7408f0416
GET /v1/drugs/abe61f77-b4fc-4f17-ab10-7bf7408f0416?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": "2,5 mg",
  "packaging": "05909990668854 ¦ Rp ¦ 46468\n28 tabl.\n05909990668861 ¦ Rp ¦ 46469\n84 tabl.",
  "substance": "Tibolonum 2.5 mg",
  "common_name": "Tibolonum",
  "pl_product_id": "100187018",
  "pozwolenie_nr": "14953",
  "auth_procedure": "MRP",
  "authorisation_validity": "Bezterminowe"
}

See everything about g03dc05.

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.