TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

KENALOG-40

TRIAMCINOLONE ACETONIDE Corticosteroid Hormone Receptor Agonists
Oncology Approved 1965-02-01
1
Indication
--
Phase 3 Trials
61
Years on Market

Details

Status
Prescription
First Approved
1965-02-01
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: TRIAMCINOLONE ACETONIDE

KENALOG-40 Approval History

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What KENALOG-40 Treats

10 indications

KENALOG-40 is approved for 10 conditions since its original approval in 1965. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Asthma
  • Atopic Dermatitis
  • Contact Dermatitis
  • Drug Hypersensitivity
  • Allergic Rhinitis
  • Serum Sickness
  • Transfusion Reaction
  • Bullous Dermatitis Herpetiformis
Source: FDA Label

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

KENALOG-40 FDA Label Details

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Indications & Usage

FDA Label (PDF)

Intramuscular Where oral therapy is not feasible, injectable corticosteroid therapy, including Kenalog-40 Injection (triamcinolone acetonide injectable suspension, USP) are indicated for intramuscular use as follows: Allergic states: Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases: Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.