Germany· DE-A57-c4f196ee437d9233
Lederlon
A medicinal product containing triamcinolone hexacetonide, registered in Germany by Esteve Pharmaceuticals Gmbh.
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
- Triamcinolone Hexacetonide
- Manufacturer
- Esteve Pharmaceuticals Gmbh
- 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
Triamcinolone hexacetonide in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NorwayHexatrioneEthypharm
- SwedenLederspan 20 mg/ml Injektionsvätska, suspensionViatris AB
- United KingdomLederspan 100mg/5ml suspension for injection vialsWyeth Pharmaceuticals
- FinlandLederspanOrifarm Oy
- CzechiaTRISPANESTEVE Pharmaceuticals GmbH, Berlín
- United StatesHexatrioneMedexus Pharma, Inc.
- IcelandLederlonWilliams & Halls ehf.*
- FranceHEXATRIONE 2 POUR CENT, suspension injectable (intra-articulaire)ETHYPHARM
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Trispan
- Czechia · Trispan
- Denmark · Lederspan, Trica
- Spain · Bluxam
- Finland · Lederspan, Trica
- France · Hexatrione
- United Kingdom (Northern Ireland) · Triamcinolone Hexacetonide Trispan
- Iceland · Lederlon, Lederspan
- Netherlands · Trispan
- Norway · Lederspan, Trica
- Portugal · Bluxam
- Sweden · Lederspan, Trica
- Slovenia · Trispan
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/075c5d17-e741-4037-bc6a-3e6f22ebf33a GET /v1/drugs/075c5d17-e741-4037-bc6a-3e6f22ebf33a?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": "Intraarticular Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Triamcinolone Hexacetonide",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about triamcinolone hexacetonide.
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.