Poland· PL-100427712
Bijuva
A progesteron und estrogen product containing estradiolum + progesteronum, registered in Poland by Theramex Ireland Limited. The same ATC class is registered in 5 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Progesteron und estrogen is registered in 5 of 19 countries.
Countries holding a registration under ATC G03FA04 (progesteron und estrogen), 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
Progesteron und estrogen · ATC G03FA04
5 / 19 countries
- Belgiumprice
- Canada
- Netherlands
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Estradiolum + Progesteronum
- Manufacturer
- Theramex Ireland Limited
- Country
- Poland (PL)
- ATC code
- G03FA04
- ATC class
- Progesteron und Estrogen
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05060632508966
- gtin05060632509055
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Progesteron und estrogen in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesBijuvaMayne Pharma
- CanadaBIJUVAKNIGHT THERAPEUTICS INC.
- SwitzerlandBijuva
- SpainBIJUVA 1 MG/100 MG CAPSULAS BLANDASTheramex Ireland Limited
- United KingdomBijuve 1mg/100mg capsulesTheramex HQ UK Ltd
- NetherlandsBijuva 1 mg/100 mg zachte capsulesTheramex Ireland Limited
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- Belgium · Duogestan
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/c0a41e3a-bf7a-45a1-9639-ba89ae03c9f0 GET /v1/drugs/c0a41e3a-bf7a-45a1-9639-ba89ae03c9f0?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": "Kapsułki miękkie",
"source": "urpl",
"strength": "1 mg + 100 mg",
"packaging": "05060632508966 ¦ Rp ¦ 140682\n28 kaps.\n05060632509055 ¦ Rp ¦ 140683\n84 kaps.",
"substance": "Estradiolum 1 mg + Progesteronum 100 mg",
"common_name": "Estradiolum + Progesteronum",
"pl_product_id": "100427712",
"pozwolenie_nr": "26471",
"auth_procedure": "DCP",
"authorisation_validity": "Bezterminowe"
}See everything about progesteron 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.