Back to search

Germany· DE-A57-ad7619394a01aade

Wick Medinait Erkältungs Für Die Nacht Für Erwachsene Und Jugendliche Ab 16 Jahren

A medicinal product containing dextromethorphan hydrobromide, doxylamine hydrogen succinate, paracetamol, ephedrine sulfate, registered in Germany by Wick Pharma Zweigniederlassung Der Procter & Gamble Gmbh.

Checked against EMA Article 57 (European Union) on

Informational only — not a medical device.

SOURCE REGISTER · DEEMA Article 57 (European Union)normalisedWick Medinait Erkältungs Für Die Nach…ATC—REGISTER NO.DE-A57-ad7619394a01aa…PACKS LISTED0CHECKEDSeptember 30, 2026

The record

At a glance

EMA Article 57 (European Union)
Active substance
Dextromethorphan Hydrobromide, Doxylamine Hydrogen Succinate, Paracetamol, Ephedrine Sulfate
Manufacturer
Wick Pharma Zweigniederlassung Der Procter & Gamble 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

Dextromethorphan hydrobromide, doxylamine hydrogen succinate, paracetamol, ephedrine sulfate in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All dextromethorphan hydrobromide, doxylamine hydrogen succinate, paracetamol, ephedrine sulfate products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Austria · Wick Medinait Erkältungs Für Die Nacht

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/6e07fb26-bd09-4057-8646-4c7083b440fa
GET /v1/drugs/6e07fb26-bd09-4057-8646-4c7083b440fa?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": "Dextromethorphan Hydrobromide, Doxylamine Hydrogen Succinate, Paracetamol, Ephedrine Sulfate",
  "atc_from_source": null,
  "authorisation_country": "Germany"
}

See everything about dextromethorphan hydrobromide, doxylamine hydrogen succinate, paracetamol, ephedrine sulfate.

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.