United States· US:59137-570_5b889707-a1a2-3fb8-e063-6294a90a3777
Hexatrione
A medicinal product containing triamcinolone hexacetonide, registered in United States by Medexus Pharma, 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
- TRIAMCINOLONE HEXACETONIDE
- Manufacturer
- Medexus Pharma, 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 · 1
- ndc1159137-570-01
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.
- United KingdomLederspan 100mg/5ml suspension for injection vialsWyeth Pharmaceuticals
- SwedenLederspan 20 mg/ml Injektionsvätska, suspensionViatris AB
- FinlandLederspanViatris Oy
- NorwayHexatrioneEthypharm
- CzechiaTRISPANESTEVE Pharmaceuticals GmbH, Berlín
- IcelandLederlonWilliams & Halls ehf.*
- FranceHEXATRIONE 2 POUR CENT, suspension injectable (intra-articulaire)ETHYPHARM
- GermanyLederlonEsteve Pharmaceuticals Gmbh
Authorised across Europe · EMA
The same active substance is authorised in 14 EEA countries. Names it is sold under:
- Austria · Trispan
- Czechia · Trispan
- Germany · Lederlon
- 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 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/1998f014-a2f8-4404-a1a1-b266d1077550 GET /v1/drugs/1998f014-a2f8-4404-a1a1-b266d1077550?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": "INTRA-ARTICULAR",
"source": "ndc",
"strength": "40",
"substance": "TRIAMCINOLONE HEXACETONIDE",
"productndc": "59137-570",
"dosage_form": "INJECTION, SUSPENSION",
"dea_schedule": null,
"strength_unit": "mg/2mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE"
}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.