United States· US:24201-201_5c279d1b-193e-46d3-a28c-43a0d3f14f96
Sodium Tetradecyl Sulfate
A medicinal product containing sodium tetradecyl sulfate, registered in United States by Hikma Pharmaceuticals USA Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- SODIUM TETRADECYL SULFATE
- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1124201201055 VIAL, GLASS in 1 CARTON (24201-201-05) / 2 mL in 1 VIAL, GLASS (24201-201-01)
- ndc1124201-201-05
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 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 FDA National Drug Code directory (United States). 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/1a9e3b05-4141-42e7-9457-2ecf6f6c17b0 GET /v1/drugs/1a9e3b05-4141-42e7-9457-2ecf6f6c17b0?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.
{
"route": "INTRAVENOUS",
"source": "ndc",
"strength": "30",
"substance": "SODIUM TETRADECYL SULFATE",
"productndc": "24201-201",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA209937",
"marketing_category": "ANDA"
}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.