France· FR:66147346
ZAMELINE 1 mg/mL, collyre en solution
A medicinal product containing diiséthionate d'hexamidine, registered in France by THEA.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- DIISÉTHIONATE D'HEXAMIDINE
- Manufacturer
- THEA
- 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
- cip13340093025721010 (2 x 5) récipient(s) multidose(s) polyéthylène basse densité (PEBD) suremballée(s)/surpochée(s) de 0,6 ml
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Diiséthionate d'hexamidine in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaZAMISEPTLaboratoires Thea, Clermont-Ferrand
- BelgiumOphtamedine 1 mg/mlLaboratoires Théa
- FinlandZamiseptLaboratoires Thea
- SwedenZamisept 1 mg/ml Ögondroppar, lösningLaboratoires THEA
- GermanyLaryngomedin NCassella-Med Gmbh & Co. Kg
- United StatesPHARMBANNER Anti-Fungal Shampoo.Shenzhen Xinxin Yunhai Technology Co., Ltd.
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Belgium · Desomedine, Hexomedine Lösung
- Bulgaria · Замидин
- Czechia · Zamisept
- Germany · Laryngomedin N, Zamidine
- Denmark · Zamisept
- Finland · Zamisept
- Greece · Zameline
- Iceland · Zameline
- Italy · Zamidine
- Luxembourg · Desomedine, Hexomedine Lösung
- Norway · Zamisept
- Poland · Zamidine
- Portugal · Zamisept
- Romania · Zamidine
- Sweden · Zamisept
- Slovakia · Zamisept
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/3e00666b-ccd9-45cb-9fe1-f5997c305256 GET /v1/drugs/3e00666b-ccd9-45cb-9fe1-f5997c305256?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": "66147346",
"date_amm": "2022-07-19",
"type_amm": "Procédure décentralisée",
"numero_ue": null,
"substance": "DIISÉTHIONATE D'HEXAMIDINE",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "collyre en solution",
"voies_administration": "ophtalmique",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about diiséthionate d'hexamidine.
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.