Belgium· BE-AMP-SAM440246-00
Nuedexta 15 mg - 9 mg
A dextromethorphan, kombinationen product containing quinidine sulfate dihydrate, registered in Belgium by Jenson Pharmaceutical Services. The same ATC class is registered in 4 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Dextromethorphan, kombinationen is registered in 4 of 19 countries.
Countries holding a registration under ATC N07XX59 (dextromethorphan, kombinationen), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 4 of them publish a price we can compare per daily dose
Dextromethorphan, kombinationen · ATC N07XX59
4 / 19 countries
- Belgiumprice
- Finlandprice
- Norwayprice
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Quinidine Sulfate Dihydrate
- Manufacturer
- Jenson Pharmaceutical Services
- Country
- Belgium (BE)
- ATC code
- N07XX59
- ATC class
- Dextromethorphan, Kombinationen
- Defined daily dose
- 40 mg, O
- 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
Dextromethorphan, kombinationen in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomKinidin 250mg DurulesAstraZeneca UK Ltd
- United StatesQuinidine gluconateEywa Pharma Inc
- FinlandChinidini SulfasOrion Corporation Orion Pharma
- Japanキニジン硫酸塩水和物
- NetherlandsKinidinesulfaat Teva 200 mg, drageesTeva Nederland B.V.
- NorwayQuinidine Sulfate epicEpic Pharma
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Hungary · Chinidin-Wagner
- Netherlands · Kinidinesulfaat Teva
- Romania · Chinidina
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/4b8d78ac-31f3-4d1b-87ff-4a5f49b413d2 GET /v1/drugs/4b8d78ac-31f3-4d1b-87ff-4a5f49b413d2?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": "Capsule, hard",
"source": "afmps",
"status": "REVOKED",
"name_en": "Nuedexta 15 mg - 9 mg",
"name_fr": "Nuedexta 15 mg - 9 mg",
"name_nl": "Nuedexta 15 mg - 9 mg",
"amp_code": "SAM440246-00",
"strengths": [
"8.6900",
"15.4100"
],
"pack_count": 2,
"substances": [
"Quinidine Sulfate Dihydrate",
"Quinidine",
"Dextromethorphan Hydrobromide",
"Dextromethorphan"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Dextromethorphan, Combinations",
"authorisation_numbers": [
"EU/1/13/833/001",
"EU/1/13/833/002"
]
}See everything about dextromethorphan, kombinationen.
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.