Germany· DE-A57-c9294a134197c0b0
Dolginox Schlaftropfen
A medicinal product containing doxylamine hydrogen succinate, registered in Germany by Dr. Theiss Naturwaren Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Doxylamine Hydrogen Succinate
- Manufacturer
- Dr. Theiss Naturwaren Gmbh
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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
Doxylamine hydrogen succinate in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesBasic Care Sleep AidAmazon.com Services LLC
- SpainDORMIDINA DOXILAMINA 12,5 mg COMPRIMIDOS RECUBIERTOS CON PELICULAEsteve Pharmaceuticals S.A.
- PolandBenosenSTADA Arzneimittel AG
- FranceDONORMYL 15 mg, comprimé effervescent sécableUPSA
- FinlandDormixOrion Corporation
- NorwayDormidina doxilaminaEsteve Pharmaceuticals S.A
- NetherlandsDoxylamine Geiser Pharma 12,5 mg poeder voor oraal gebruikGeiser Pharma S.L.
- BelgiumNavalit 10 mg - 10 mgEFFIK Benelux
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Hoggar Night
- Cyprus · Hoggar Night
- Spain · Dormidina, Dormigen
- Finland · Dormix
- France · Donormyl, Doxylamine Arrow Conseil
- Greece · Hoggar Night
- Croatia · Hoggar
- Hungary · Hoggar
- Malta · Doxylamine Krka, Normodorm
- Norway · Zonat
- Poland · Benosen, Doksylamina Geiser
- Portugal · Dormidina, Hoggar
- Slovenia · Noctiben Mea
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 EMA Article 57 (European Union). 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/f28c2f80-53d1-4aa4-a25c-00d3e880645f GET /v1/drugs/f28c2f80-53d1-4aa4-a25c-00d3e880645f?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.
{
"pzn": null,
"route": "Oral Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Doxylamine Hydrogen Succinate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about doxylamine hydrogen succinate.
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.