Poland· PL-100509846
Femoston mini
A dydrogesteron und estrogen product containing estradiolum + dydrogesteronum, registered in Poland by InPharm Sp. z o.o.. The same ATC class is registered in 9 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Dydrogesteron und estrogen is registered in 9 of 19 countries.
Countries holding a registration under ATC G03FA14 (dydrogesteron und estrogen), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 6 of them publish a price we can compare per daily dose
Dydrogesteron und estrogen · ATC G03FA14
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Estradiolum + Dydrogesteronum
- Manufacturer
- InPharm Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- G03FA14
- ATC class
- Dydrogesteron und Estrogen
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05909991561345
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
11 interactions on record for dydrogesteron und estrogen.
Mechanism, severity and management for each pair, from a commercially licensed source — included with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Dydrogesteron und estrogen · interactions on record
11 records
11 more interactions with mechanism and management, from a commercially licensed source.
Sign in to checkSame medicine, other countries
Dydrogesteron und estrogen in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomEstradiol 1mg / Dydrogesterone 10mg tabletsExeltis UK Ltd
- NetherlandsFemoston 1/10, filmomhulde tablettenAbbott B.V.
- SwedenFemoston 1 mg + 1 mg/10 mg Filmdragerad tablettEbb Medical AB
- IrelandFemoston 1/10mg film-coated tabletsTheramex Ireland Limited
- NorwayFemostonViatris
- SwitzerlandFemoston
- SpainFEMFASCON 1 MG/10 MG COMPRIMIDOS RECUBIERTOS CON PELICULATheramex Ireland Limited
- GermanyFemoston ContiTheramex Ireland Limited
Authorised across Europe · EMA
The same active substance is authorised in 24 EEA countries. Names it is sold under:
- Austria · Femoston, Femoston Conti
- Belgium · Femoston, Femoston 2/10
- Cyprus · Femoston
- Czechia · Femoston, Femoston Conti
- Germany · Femoston, Femoston Conti
- Denmark · Femoston, Femoston Conti
- Estonia · Femoston, Femoston Conti
- Spain · Femfascon, Femoston
- Finland · Femoston, Femoston Conti
- France · Climaston
- Greece · Femaston
- Croatia · Femoston, Femoston Conti
- Ireland · Femoston, Femoston-Conti
- Italy · Femoston, Femoston Conti
- Lithuania · Femoston, Femoston Conti
- Luxembourg · Femoston, Femoston Conti
- Latvia · Femoston, Femoston Conti
- Malta · Femoston, Femoston-Conti
- Netherlands · Femoston, Femoston Continu
- Norway · Femoston, Femostonconti
- Portugal · Femoston
- Sweden · Femoston, Femostonconti
- Slovenia · Femphascon Conti
- Slovakia · Femoston, Femoston Conti
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/fa67e28d-a025-4c92-8021-bbd6ae84ca3f GET /v1/drugs/fa67e28d-a025-4c92-8021-bbd6ae84ca3f?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 powlekane",
"source": "urpl",
"strength": "0,5 mg + 2,5 mg",
"packaging": "05909991561345 ¦ Rp ¦ 159447\n28 tabl.",
"substance": "Estradiolum 0.5 mg + Dydrogesteronum 2.5 mg",
"common_name": "Estradiolum + Dydrogesteronum",
"pl_product_id": "100509846",
"pozwolenie_nr": "438/24",
"auth_procedure": "IR",
"authorisation_validity": "2029-12-17"
}See everything about dydrogesteron und estrogen.
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.