Poland· PL-100545128
Enspryng
A satralizumab product containing satralizumabum, registered in Poland by Roche Registration GmbH. The same ATC class is registered in 13 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Satralizumab is registered in 13 of 19 countries.
Countries holding a registration under ATC L04AC19 (satralizumab), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 8 of them publish a price we can compare per daily dose
Satralizumab · ATC L04AC19
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
URPL (Poland)- Active substance
- Satralizumabum
- Manufacturer
- Roche Registration GmbH
- Country
- Poland (PL)
- ATC code
- L04AC19
- ATC class
- Satralizumab
- Defined daily dose
- 4.3 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin07613326101752
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
115 interactions on record for satralizumab.
Graded by severity as the source publishes them — 35 severe. 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
Satralizumab · interactions on record
115 records
- 35 severe
- 74 moderate
- 6 minor
Most severe, free to view
- CladribineL01BB04severe
- RituximabL01FA01severe
- RituximabL01XC02severe
- Talimogene laherparepvecL01XL02severe
- 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
Satralizumab in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaENSPRYNGRoche Registration GmbH, Grenzach-Wyhlen
- BelgiumEnspryng 120 mgRoche Registration
- SpainENSPRYNG 120 mg SOLUCION INYECTABLE EN JERINGA PRECARGADARoche Registration Gmbh
- United KingdomEnspryng 120mg/1ml solution for injection pre-filled syringesRoche Products Ltd
- SwedenEnspryng 120 mg Injektionsvätska, lösning i förfylld sprutaRoche Registration GmbH
- FinlandEnspryngRoche Registration GmbH
- Japanサトラリズマブ(遺伝子組換え)中外製薬
- United StatesEnspryngGenentech, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Enspryng, Enspryng Pre-Filled Pen Pre-Filled Pen
- Liechtenstein · Enspryng, Enspryng Pre-Filled Pen Pre-Filled Pen
- Norway · Enspryng, Enspryng Pre-Filled Pen Pre-Filled Pen
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/dd61b3cb-640f-4e09-b95f-3656c7443fe9 GET /v1/drugs/dd61b3cb-640f-4e09-b95f-3656c7443fe9?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 we wstrzykiwaczu",
"source": "urpl",
"strength": "120 mg",
"packaging": "07613326101752 ¦ Rpz ¦ EU/1/21/1559/003 ¦ 168468\n1 wstrzyk. 1 ml\nRpz ¦ EU/1/21/1559/004 ¦ 168469\n3 wstrzyk. 1 ml",
"substance": "Satralizumabum 120 mg",
"common_name": "Satralizumabum",
"pl_product_id": "100545128",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about satralizumab.
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.