Belgium· BE-AMP-SAM039277-00
Paranausine 80 mg
A medicinal product containing dimenhydrinate, registered in Belgium by EG.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Dimenhydrinate
- Manufacturer
- EG
- Country
- Belgium (BE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 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
Dimenhydrinate in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesAirmit AceSato Pharmaceutical Co., Ltd.
- GermanyDimenhydrinat AlAliud Pharma Gmbh
- CanadaANTI-NAUSEANTVITA HEALTH PRODUCTS INC
- SpainBIODRAMINA 100 mg SUPOSITORIOSUriach Aquilea Otc, S.L.
- NorwayDimenhydrinat aluidAliud Pharma
- PolandAviomarinTeva Pharmaceuticals Polska Sp. z o.o.
- FranceNAUSICALM 15,7 mg ENFANTS, sirop en sachetBROTHIER
- United KingdomDimenhydrinate 12.5mg/5ml oral solutionSpecial Order
Authorised across Europe · EMA
The same active substance is authorised in 20 EEA countries. Names it is sold under:
- Austria · Travelgum, Vertirosan
- Bulgaria · Вомакур, Дименхидринат Актавис
- Cyprus · Oriens Vom, Travelgum 20mg
- Germany · Dimenhydrinat Al, Dimenhydrinat Hameln
- Denmark · Dimenhydrinat Galenica
- Spain · Biodramina, Biodramina Infantil
- France · Nausicalm, Nausicalm Adultes
- United Kingdom (Northern Ireland) · Travlese
- Greece · Travelgum 20mg, Vomex-A
- Croatia · Dramina
- Hungary · Daedalon, Daedalon Kid
- Italy · Lomarin, Novago
- Luxembourg · Dimenhydrinat Hameln, Vomex A
- Latvia · Vertirosan
- Malta · Biodramina, Vomidrine
- Poland · Aviomarin
- Portugal · Draminal, Enjomin
- Romania · Oriens
- Sweden · Calma
- Slovenia · Dramina
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 FAMHP / AFMPS (Belgium). 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/016c0b17-0d39-483b-931b-5b076978ad4b GET /v1/drugs/016c0b17-0d39-483b-931b-5b076978ad4b?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": "Tablet",
"source": "afmps",
"status": "REVOKED",
"name_en": "Paranausine 80 mg",
"name_fr": "Paranausine 80 mg",
"name_nl": "Paranausine 80 mg",
"amp_code": "SAM039277-00",
"strengths": [
"80.0000"
],
"pack_count": 1,
"substances": [
"Dimenhydrinate"
],
"medicine_type": "ALLOPATHIC",
"atc_description": null,
"authorisation_numbers": [
"0616S 0167F003"
]
}See everything about dimenhydrinate.
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.