Finland· FI-REL-REL9642
Premelle Cyklisk
A medroxyprogesteron und estrogen product containing estrogens conjugated (usp) + medroxyprogesterone acetate, registered in Finland by Wyeth Medica Ireland. The same ATC class is registered in 2 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Medroxyprogesteron und estrogen is registered in 2 of 19 countries.
Countries holding a registration under ATC G03FB06 (medroxyprogesteron und estrogen), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 2 of them publish a price we can compare per daily dose
Medroxyprogesteron und estrogen · ATC G03FB06
2 / 19 countries
- Finlandprice
- Polandprice
The record
At a glance
Fimea (Finland)- Active substance
- Estrogens conjugated (usp) + Medroxyprogesterone acetate
- Manufacturer
- Wyeth Medica Ireland
- Country
- Finland (FI)
- ATC code
- G03FB06
- ATC class
- Medroxyprogesteron und Estrogen
- Reimbursed
- Not published by this register
- Source register
- Fimea (Finland)
- Last checked
- September 27, 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
Medroxyprogesteron und estrogen in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomConjugated oestrogens 300microgram / Medroxyprogesterone 1.5mg modified-release tabletsPfizer Ltd
- United StatesPremproWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- United Kingdom (Northern Ireland) · Conjugated Oestrogens/Medroxyprogesterone Acetate Pfizer, Premique Low Dose
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 Fimea (Finland). 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/dc0962d1-d261-43e9-83a9-2f26b1b7feff GET /v1/drugs/dc0962d1-d261-43e9-83a9-2f26b1b7feff?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.
{
"ddd": null,
"form": "tabletti, kalvopäällysteinen",
"route": null,
"ddd_unit": null,
"strength": null,
"atc_label": "medroksiprogesteroni ja estrogeeni",
"ma_number": "12993",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL9642",
"authorised_at": "1998-08-10"
}See everything about medroxyprogesteron 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.