France· FR:67456915
TECHNESCAN DMSA 1,2 mg trousse pour préparation radiopharmaceutique
A medicinal product containing succimer, registered in France by CURIUM NETHERLANDS (PAYS-BAS).
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- SUCCIMER
- Manufacturer
- CURIUM NETHERLANDS (PAYS-BAS)
- Country
- France (FR)
- ATC code
- —
- Reimbursed
- No
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
- cip1334009564458755 flacon(s) multidoses en verre de 31,4 mg
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Succimer in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsTechnescan DMSA, 1,2 mg kit voor radiofarmaceutisch preparaatCurium Netherlands B.V.
- United KingdomChemet 100mg capsulesImported (United States)
- CzechiaSUCCICAPTAL
- GermanyDmsa RotopRotop Pharmaka Gmbh
- IrelandRENOCIS 1 mg kit for radiopharmaceutical preparationCIS bio International
- United StatesChemetRecordati Rare Diseases, Inc.
- SwitzerlandSuccicaptal, KapselnCuratis AG
- NorwaySuccicaptalLaboratoires SERB
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Czechia · Technescan Dmsa
- Germany · Dmsa Rotop, Technescan Dmsa
- Spain · Dmsa Technescan Curium Pharma Spain
- Italy · Renocis
- Malta · Succicaptal
- Sweden · Renocis
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/88c2d8fb-47bb-4d18-a06c-7320fefb04b1 GET /v1/drugs/88c2d8fb-47bb-4d18-a06c-7320fefb04b1?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": "67456915",
"date_amm": "2005-01-05",
"type_amm": "Procédure nationale",
"numero_ue": null,
"substance": "SUCCIMER",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "trousse pour préparation radiopharmaceutique",
"voies_administration": "intraveineuse",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about succimer.
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.