Spain· ES:73-948-10-CIP
MICTONORM 30 MG CAPSULAS DE LIBERACION MODIFICADA
A medicinal product containing propiverina, registered in Spain by Herbacos Recordati S.R.O..
Checked against AEMPS CIMA (Spain) on
Informational only — not a medical device.
The record
At a glance
AEMPS CIMA (Spain)- Active substance
- propiverina
- Manufacturer
- Herbacos Recordati S.R.O.
- Country
- Spain (ES)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- AEMPS CIMA (Spain)
- Last checked
- June 3, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Propiverina in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaMICTONORM UNOHerbacos Recordati s.r.o., Pardubice
- United KingdomDetrunorm XL 30mg capsulesConsilient Health Ltd
- BelgiumMictonorm Uno 30 mgConsilient Health
- IrelandDetrunorm XL 30 mg Modified-Release CapsulesAPOGEPHA Arzneimittel GmbH
- SwitzerlandMictonorm 30 mg, gélules à libération modifiéeLabatec Pharma SA
- GermanyMictonettenApogepha Arzneimittel Gmbh
- CanadaMICTORYLDUCHESNAY INC
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Mictonorm
- Belgium · Mictonet, Mictonorm
- Czechia · Mictonetten, Mictonorm
- Germany · Mictonetten, Mictonorm
- United Kingdom (Northern Ireland) · Aponorm Xl, Detrunorm
- Greece · Mictonorm, Mictonorm Uno
- Croatia · Detrunorm, Detrunorm Xr
- Ireland · Detrunorm, Detrunorm Xl
- Italy · Mictonorm
- Luxembourg · Mictonorm Forte, Mictonorm Uno
- Portugal · Mictonorm Od
- Slovenia · Detrunorm
- Slovakia · Mictonetten, Mictonorm
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 AEMPS CIMA (Spain). 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/bc5c0c5b-9c28-4c24-84cb-87b6dd119219 GET /v1/drugs/bc5c0c5b-9c28-4c24-84cb-87b6dd119219?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.
{
"cpresc": "Medicamento Sujeto A Prescripción Médica",
"estado": "{\"aut\":1698404920000}",
"nregistro": "73-948-10-CIP",
"substance": "propiverina"
}See everything about propiverina.
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.