France· FR:60385682
DANTRIUM 100 mg, gélule
A dantrolene product containing dantrolène sodique, registered in France by NORGINE, on the national reimbursement list. The same ATC class is registered in 16 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
Dantrolene is registered in 16 of 19 countries.
Countries holding a registration under ATC M03CA01 (dantrolene), each read from that country’s own register.
- This record: France, from Base de données publique des médicaments — BDPM (France)
- 9 of them publish a price we can compare per daily dose
Dantrolene · ATC M03CA01
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of dantrolene costs, country by country.
Normalised to the WHO defined daily dose (0.1 g), the median price runs from $1.64 in United States to $5.92 in Finland — a ×3.6 gap.
- 2 markets with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
- US figures are pharmacy acquisition cost (CMS NADAC), not retail
Dantrolene · price per daily dose (0.1 g)
USD · FX 28 Sept 2026
- FI Finland$5.92
- US United States$1.64 (acquisition cost)
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- DANTROLÈNE SODIQUE
- Manufacturer
- NORGINE
- Country
- France (FR)
- ATC code
- M03CA01
- ATC class
- Dantrolene
- Defined daily dose
- 0.1 g, O
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip133400932156177plaquette(s) thermoformée(s) PVC-aluminium de 30 gélule(s)EUR 10.76
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
93 interactions on record for dantrolene.
Graded by severity as the source publishes them — 16 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
Dantrolene · interactions on record
93 records
- 16 severe
- 60 moderate
- 17 info
Most severe, free to view
- Levonorgestrel and ethinylestradiolG03AA07severe
- Desogestrel and ethinylestradiolG03AA09severe
- Drospirenone and ethinylestradiolG03AA12severe
- EthinylestradiolG03CA01severe
- 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
Dantrolene in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United Statesdantrolene sodiumEndo USA, Inc.
- United KingdomDantrium 100mg capsulesWaymade Healthcare Plc
- IrelandDantrium 100 mg CapsulesNorgine B.V.
- SwitzerlandAgilus 120 mg, Pulver zur Herstellung einer InjektionslösungNorgine AG
- CanadaDANTRIUM CAPSULESENDO OPERATIONS LTD.
- NetherlandsAgilus 120 mg poeder voor oplossing voor injectieNorgine B.V.
- FinlandAgilusOrifarm Oy
- CzechiaAGILUSNorgine B.V., Amsterdam
Authorised across Europe · EMA
The same active substance is authorised in 9 EEA countries. Names it is sold under:
- Belgium · Dantrium Iv
- Germany · Dantamacrin, Dantrolen I.V.
- United Kingdom (Northern Ireland) · Agilus, dantrium
- Ireland · Dantrium
- Iceland · Agilus
- Italy · Dantrium
- Liechtenstein · Agilus
- Netherlands · Dantrium
- Norway · Agilus
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/ee8e71a3-ec88-435f-b952-d5841529d346 GET /v1/drugs/ee8e71a3-ec88-435f-b952-d5841529d346?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": "60385682",
"date_amm": "1978-06-29",
"type_amm": "Procédure nationale",
"numero_ue": null,
"substance": "DANTROLÈNE SODIQUE",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "gélule",
"voies_administration": "orale",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about dantrolene.
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.