Poland· PL-100022180
Enema
A sodium phosphate product containing dinatrii phosphas dodecahydricus + natrii dihydrogenophosphas monohydricus, registered in Poland by Laboratorium Galenowe Olsztyn Sp. z o.o.. The same ATC class is registered in 8 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Sodium phosphate is registered in 8 of 19 countries.
Countries holding a registration under ATC A06AG01 (sodium phosphate), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 5 of them publish a price we can compare per daily dose
Sodium phosphate · ATC A06AG01
8 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Ireland
- Netherlands
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Dinatrii phosphas dodecahydricus + Natrii dihydrogenophosphas monohydricus
- Manufacturer
- Laboratorium Galenowe Olsztyn Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- A06AG01
- ATC class
- Sodium phosphate
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05909990298716
- gtin05909990298723
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same class
Other records under A06AG01
Sodium phosphate, as other registers publish it.
- CzechiaCASINEMACasen Recordati, S.L., Utebo, Zaragoza
- BelgiumCleen Enema 11 g - 24 gCasen Recordati
- NetherlandsCleenema 139,1 mg/ml / 31,7 mg/ml, oplossing voor rectaal gebruikCasen Recordati, S.L.
- DenmarkCleenema Klar-til-brugCasen Recordati, S.L.
- IrelandCleenema Ready-to-Use 21.4 g/9.4 g EnemaCasen-Recordati S.L.
- BelgiumColex KlysmaTramedico
- NetherlandsColex klysma 31,8 mg/ml / 139,1 mg/ml, oplossing voor rectaal gebruikTramedico B.V.
- DenmarkFosfat "SAD"Amgros I/S
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/232ff6e9-5aa2-4531-944e-dff4be3b13ee GET /v1/drugs/232ff6e9-5aa2-4531-944e-dff4be3b13ee?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 doodbytniczy",
"source": "urpl",
"strength": "(32,2 mg + 139 mg)/ml",
"packaging": "05909990298716 ¦ OTC ¦ 3672\n1 butelka 150 ml\n05909990298723 ¦ Lz ¦ 13833\n50 butelek 150 ml",
"substance": "Dinatrii phosphas dodecahydricus 32.2 mg/ml + Natrii dihydrophosphas 139 mg/ml",
"common_name": "Dinatrii phosphas dodecahydricus + Natrii dihydrogenophosphas monohydricus",
"pl_product_id": "100022180",
"pozwolenie_nr": "02987",
"auth_procedure": "NAR",
"authorisation_validity": "Bezterminowe"
}See everything about 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.