Germany· DE-A57-548cc84571d9eb75
Pemetrexed Zentiva
A medicinal product containing pemetrexed disodium hemipentahydrate, registered in Germany by Zentiva Pharma Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Pemetrexed Disodium Hemipentahydrate
- Manufacturer
- Zentiva Pharma Gmbh
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- August 5, 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
Pemetrexed disodium hemipentahydrate in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesPemetrexedSagent Pharmaceuticals
- BelgiumCiambra 100 mgMenarini International Operations Luxembourg
- FinlandCiambraMenarini International Operations Luxembourg S.A.
- CzechiaARMISARTEActavis Group PTC ehf., Hafnarfjördur
- IrelandPemetrexed Clonmel 25 mg/ml concentrate for solution for infusionClonmel Healthcare Ltd
- SwedenPemetrexed Zentiva 10 mg/ml Infusionsvätska, lösningZentiva k.s.
Authorised across Europe · EMA
The same active substance is authorised in 10 EEA countries. Names it is sold under:
- Austria · Pemetrexed Zentiva
- Denmark · Pemetrexed Zentiva
- Spain · Pemetrexed Prasfarma
- Finland · Pemetrexed Zentiva
- France · Pemetrexed Zentiva
- United Kingdom (Northern Ireland) · Pemetrexed Zentiva
- Netherlands · Pemetrexed Zentiva
- Norway · Pemetrexed Zentiva
- Portugal · Pemetrexedo Stada
- Sweden · Pemetrexed Zentiva
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 EMA Article 57 (European Union). 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/f4f2b619-ce6d-4e94-ac6b-110a5bd70d4c GET /v1/drugs/f4f2b619-ce6d-4e94-ac6b-110a5bd70d4c?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.
{
"pzn": null,
"route": "Intravenous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Pemetrexed Disodium Hemipentahydrate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about pemetrexed disodium hemipentahydrate.
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.