Germany· DE-A57-e00f667fb44c32f0
Fibrovein
A medicinal product containing sodium tetradecyl sulfate, registered in Germany by Std Pharmaceutical (Ireland) Ltd.
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
- Sodium Tetradecyl Sulfate
- Manufacturer
- Std Pharmaceutical (Ireland) Ltd
- 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
Sodium tetradecyl sulfate in 9 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomFibro-Vein 0.2% solution for injection 5ml vialsSTD Pharmaceutical Products Ltd
- CzechiaFIBROVEINSTD Pharmaceutical (Ireland) Limited, Dublin
- FranceFIBROVEIN 0,2 %, solution injectableSTD PHARMACEUTICAL (IRELAND) (IRLANDE)
- PolandFibroveinSTD Pharmaceutical (Ireland) Limited
- SpainVEINFIBRO 0,2 % SOLUCION INYECTABLEStd Pharmaceutical (Ireland) Limited
- IrelandFibrovein 0.2% Solution for InjectionSTD Pharmaceutical (Ireland) Limited
- CanadaTROMBOJECT 1%OMEGA LABORATORIES LIMITED
- NorwayFibroveinSTD Pharmaceutical Products
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Spain · Veinfibro
- France · Fibrovein, Trombovar
- Ireland · Fibrovein
- Italy · Fibrovein
- Poland · Fibrovein
- Romania · Fibrovein
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/409b3761-9013-458f-9515-24c49bbdc954 GET /v1/drugs/409b3761-9013-458f-9515-24c49bbdc954?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": "Intravenous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Sodium Tetradecyl Sulfate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about sodium tetradecyl 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.