Germany· DE-A57-154c699d074ab999
Erypo Fs
A epoetin alfa product containing epoetin alfa, registered in Germany by Janssen-Cilag Gmbh. The same ATC class is registered in 2 of our 19 countries.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
Where it is registered
Epoetin alfa is registered in 2 of 19 countries.
Countries holding a registration under ATC EPOETIN ALFA (epoetin alfa), each read from that country’s own register.
- This record: Germany, from EMA Article 57 (European Union)
Epoetin alfa · ATC EPOETIN ALFA
2 / 19 countries
- Germany
- United Kingdom
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Epoetin Alfa
- Manufacturer
- Janssen-Cilag Gmbh
- Country
- Germany (DE)
- ATC code
- EPOETIN ALFA
- ATC class
- EPOETIN ALFA
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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 class
Other records under EPOETIN ALFA
Epoetin alfa, as other registers publish it.
- United KingdomBinocrit 1,000units/0.5ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 10,000units/1ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 2,000units/1ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 20,000units/0.5ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 3,000units/0.3ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 30,000units/0.75ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 4,000units/0.4ml solution for injection pre-filled syringesSandoz Ltd
- United KingdomBinocrit 40,000units/1ml solution for injection pre-filled syringesSandoz Ltd
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/f07a1551-0271-4784-a435-ad60f3f3ca50 GET /v1/drugs/f07a1551-0271-4784-a435-ad60f3f3ca50?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": "Cutaneous Use ,Intravenous Use ,Parenteral Use ,Subcutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Epoetin Alfa",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about epoetin alfa.
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.