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France· FR:67657117

DOXYLAMINE TEVA CONSEIL 15 mg, comprimé pelliculé sécable

A medicinal product containing hydrogénosuccinate de doxylamine, registered in France by TEVA SANTE.

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedDOXYLAMINE TEVA CONSEIL 15 mg, compri…ATC—REGISTER NO.FR:67657117PACKS LISTED1CHECKEDSeptember 12, 2026

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
HYDROGÉNOSUCCINATE DE DOXYLAMINE
Manufacturer
TEVA SANTE
Country
France (FR)
ATC code
—
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400926630706
    tube(s) polypropylène de 10 comprimé(s)

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Hydrogénosuccinate de doxylamine in 9 other countries

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

All hydrogénosuccinate de doxylamine products

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
  • Germany · Dolginox Schlaftropfen, Doxylamin Dexcel
  • Spain · Dormidina, Dormigen
  • Finland · Dormix
  • 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 Base de données publique des médicaments — BDPM (France). 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/fece9f54-17f4-4e79-beb4-f5d7e7919a1d
GET /v1/drugs/fece9f54-17f4-4e79-beb4-f5d7e7919a1d?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.

{
  "cis": "67657117",
  "date_amm": "2012-09-06",
  "type_amm": "Procédure nationale",
  "numero_ue": null,
  "substance": "HYDROGÉNOSUCCINATE DE DOXYLAMINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "comprimé pelliculé sécable",
  "voies_administration": "orale",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about hydrogénosuccinate de doxylamine.

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.