Active substance
Triamcinolone hexacetonide
- US FDA 1
- WHO EML 1
- Safety 1
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
|---|---|---|---|---|---|
| ARISTOSPAN | 5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; 20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | injectable · injection | ETHYPHARM | Discontinued | 29 Jul 1969 |
WHO WHO Model List of Essential Medicines (2025)
- 29.3. Medicines for juvenile joint diseases · complementary
Juvenile idiopathic arthritis
Parenteral > Locoregional injections > Intra-articular: 20 mg per mL in vial
Safety signals and safety-related labeling changes
- US FDA 5 Jun 2024 ARISTOSPAN — safety-related labeling change
Labeling sections changed: Warnings and Precautions
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.