France· FR:69326436
ENSPRYNG 120 mg, solution injectable en seringue préremplie
A satralizumab product containing satralizumab, registered in France by ROCHE REGISTRATION (ALLEMAGNE), on the national reimbursement list. The same ATC class is registered in 13 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) 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: France, from Base de données publique des médicaments — BDPM (France)
- 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
Base de données publique des médicaments — BDPM (France)- Active substance
- SATRALIZUMAB
- Manufacturer
- ROCHE REGISTRATION (ALLEMAGNE)
- Country
- France (FR)
- ATC code
- L04AC19
- ATC class
- Satralizumab
- Defined daily dose
- 4.3 mg, P
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip1334009302344331 seringue(s) préremplie(s) poly(ferrocénylsilane) (PFS) de 1 mlEUR 7.56
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.
- IrelandEnspryng 120 mg solution for injection in pre-filled syringeRoche Registration GmbH
- NetherlandsEnspryng 120 mg, oplossing voor injectie in voorgevulde spuitRoche Registration GmbH
- CzechiaENSPRYNGRoche Registration GmbH, Grenzach-Wyhlen
- BelgiumEnspryng 120 mgRoche Registration
- FinlandEnspryngRoche Registration GmbH
- Japanサトラリズマブ(遺伝子組換え)中外製薬
- PolandEnspryngRoche Registration GmbH
- 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 Base de données publique des médicaments — BDPM (France). 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/e00d7e90-9473-4ad8-b5d1-9a9ac62105ab GET /v1/drugs/e00d7e90-9473-4ad8-b5d1-9a9ac62105ab?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.
{
"cis": "69326436",
"date_amm": "2021-06-24",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/21/1559",
"substance": "SATRALIZUMAB",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "solution injectable",
"voies_administration": "sous-cutanée",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}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.