United Kingdom· GB-APID-22798011000001100
Fibrovein 0.2% solution for injection 5ml vials
A medicinal product containing sodium tetradecyl sulfate, registered in United Kingdom by STD Pharmaceutical Products Ltd.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Sodium tetradecyl sulfate
- Manufacturer
- STD Pharmaceutical Products Ltd
- Country
- United Kingdom (GB)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 4
- gtin5019363102011
- gtin05019363102011
- gtin05019363102158
- gtin5019363102158
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.
- CzechiaFIBROVEINSTD Pharmaceutical (Ireland) Limited, Dublin
- FranceFIBROVEIN 0,2 %, solution injectableSTD PHARMACEUTICAL (IRELAND) (IRLANDE)
- IrelandFibrovein 0.2% Solution for InjectionSTD Pharmaceutical (Ireland) Limited
- PolandFibroveinSTD Pharmaceutical (Ireland) Limited
- SpainVEINFIBRO 0,2 % SOLUCION INYECTABLEStd Pharmaceutical (Ireland) Limited
- CanadaTROMBOJECT 1%OMEGA LABORATORIES LIMITED
- NorwayFibroveinSTD Pharmaceutical Products
- GermanyFibroveinStd Pharmaceutical (Ireland) Ltd
Authorised across Europe · EMA
The same active substance is authorised in 7 EEA countries. Names it is sold under:
- Germany · Fibrovein
- 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 NHS dm+d (United Kingdom). 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/ec887ff8-e931-442c-b23f-9f7aae213327 GET /v1/drugs/ec887ff8-e931-442c-b23f-9f7aae213327?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.
{
"apid": "22798011000001100",
"desc": "Fibrovein 0.2% solution for injection 5ml vials (STD Pharmaceutical Products Ltd)",
"form": "Solution for injection",
"vpid": "4515211000001107",
"source": "dmd",
"vtm_id": "777581005",
"strength": "2 mg",
"substance": "Sodium tetradecyl sulfate",
"ingredient": "Sodium tetradecyl sulfate",
"supplier_code": "190301000001106"
}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.