Germany· DE-A57-280120fd117da73f
Okrido
A medicinal product containing prednisolone sodium phosphate, registered in Germany by Pharmapol Arzneimittelvertrieb-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
- Prednisolone Sodium Phosphate
- Manufacturer
- Pharmapol Arzneimittelvertrieb-Gmbh
- Country
- Germany (DE)
- ATC code
- —
- 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 medicine, other countries
Prednisolone sodium phosphate in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesOrapredAdvanz Pharma (US) Corp.
- SwedenPrednisolon Evolan 31,25 mg RektallösningEvolan Pharma AB
- NorwayOkridoPharmapol
- IrelandMinims Prednisolone Sodium Phosphate 0.5% w/v Eye Drops, SolutionBausch + Lomb Ireland Limited
- FinlandPrednimentFerring A/S
- CanadaMINIMS PREDNISOLONE SODIUM PHOSPHATEBAUSCH & LOMB INC
- United KingdomPrednisolone 5mg soluble tablets sugar freeSovereign Medical Ltd
Authorised across Europe · EMA
The same active substance is authorised in 11 EEA countries. Names it is sold under:
- Cyprus · Adelone, Prednisolone Bausch+lomb
- Denmark · Prednisolon Unimedic
- Spain · Prednisolona Minims
- Finland · Provistopto
- United Kingdom (Northern Ireland) · Prednisolone Rph Pharmaceuticals, Prednisolone Sodium Phosphate Aspire Pharma
- Greece · Adelone, Cordeslon
- Ireland · Minims
- Malta · Minims, Provist-Opto
- Netherlands · Minims Prednisolondinatriumfosfaat Bausch Health Ireland, Provist-Opto
- Norway · Prednisolon Unimedic
- Sweden · Prednisolon Evolan, Prednisolon Unimedic
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/43dc0873-6ec0-4661-8f53-b3f4f2368d20 GET /v1/drugs/43dc0873-6ec0-4661-8f53-b3f4f2368d20?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": "Oral Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Prednisolone Sodium Phosphate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about prednisolone sodium phosphate.
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.