Poland· PL-100452882
Ovamex
A ganirelix product containing ganirelixum, registered in Poland by Theramex Ireland Limited. The same ATC class is registered in 17 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Ganirelix is registered in 17 of 19 countries.
Countries holding a registration under ATC H01CC01 (ganirelix), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 10 of them publish a price we can compare per daily dose
Ganirelix · ATC H01CC01
17 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Spainprice
- Sweden
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
URPL (Poland)- Active substance
- Ganirelixum
- Manufacturer
- Theramex Ireland Limited
- Country
- Poland (PL)
- ATC code
- H01CC01
- ATC class
- Ganirelix
- Defined daily dose
- 0.25 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05060632509246
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
7 interactions on record for ganirelix.
Graded by severity as the source publishes them — 7 moderate. Severity grades are free for everyone; mechanism and management come 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
Ganirelix · interactions on record
7 records
- 7 moderate
Most severe, free to view
- Chorionic gonadotrophinG03GA01moderate
- Menotropin HMGG03GA02moderate
- UrofollitropinG03GA04moderate
- GonadorelinH01CA01moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Ganirelix in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaGANIRELIX GEDEON RICHTERGedeon Richter Plc., Budapešť
- SpainASTARTE 0,25 MG/0,5 ML SOLUCION INYECTABLE EN JERINGA PRECARGADA EFGGp Pharm S.A.
- SwedenFyremadel 0,25 mg/0,5 ml Injektionsvätska, lösning i förfylld sprutaSun Pharmaceutical Industries Europe B.V.
- BelgiumFyremadel 0.25 mg/0.5 mlSun Pharmaceutical Industries Europe
- NorwayGanirelix Gedeon RichterGedeon Richter Plc
- IcelandOrgalutranN.V. Organon*
- United StatesFyremadelFerring Pharmaceuticals Inc.
- FinlandFyremadelSun Pharmaceutical Industries Europe B.V.
Authorised across Europe · EMA
The same active substance is authorised in 25 EEA countries. Names it is sold under:
- Austria · Ganirelix Astro, Ganirelix Theramex
- Belgium · Fyremadel, Ovamex
- Bulgaria · Ganirelix Theramex
- Czechia · Fyremadel
- Germany · Fyremadel, Ganiran
- Denmark · Fyremadel, Ganirelix Orifarm
- Estonia · Ganirelix Theramex
- Spain · Astarté, Fyremadel
- Finland · Fyremadel, Ganirelix Orifarm
- France · Fyremadel, Ganirelix Eg
- United Kingdom (Northern Ireland) · Fyremadel
- Greece · Fyremadel, Ovamex
- Croatia · Ganireliks Theramex
- Hungary · Ganirelix Theramex
- Iceland · Ganirelix, Ganirelix Gedeon Richter
- Italy · Fyremadel, Ovamex
- Liechtenstein · Ganirelix, Ganirelix Gedeon Richter
- Lithuania · Ganirelix Theramex
- Latvia · Ganirelix Theramex
- Netherlands · Fyremadel, Ganirelix Fagron
- Norway · Fyremadel, Ganirelix
- Portugal · Astarté, Fyremadel
- Sweden · Fyremadel, Ganirelix Orifarm
- Slovenia · Ganireliks Theramex
- Slovakia · Fyremadel, Ganirelix Theramex
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/febd9f87-21d8-4ce1-885b-a8ff6f20430d GET /v1/drugs/febd9f87-21d8-4ce1-885b-a8ff6f20430d?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": "Roztwór do wstrzykiwań w ampułko-strzykawce",
"source": "urpl",
"strength": "0,25 mg/0,5 ml",
"packaging": "05060632509246 ¦ Rpz ¦ 146348\n1 amp.-strzyk. 0,5 ml",
"substance": "Ganirelixi acetas 0,25 mg/0,5 ml",
"common_name": "Ganirelixum",
"pl_product_id": "100452882",
"pozwolenie_nr": "27248",
"auth_procedure": "DCP",
"authorisation_validity": "2027-08-04"
}See everything about ganirelix.
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.