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Brand-name prescription medicine

Triesence

Generic name: Triamcinolone acetonide

FDA application holder: Harrow Eye

Strengths and generic versions Official label

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

At a glance

1Strengths and forms
24Same medicine, other names
2007FDA approval
0Recalls (FDA reports)

Quick answers

What is Triesence?
Triesence is a brand name of Triamcinolone acetonide, a prescription medicine. The FDA NDC Directory lists 2 Triesence products in 1 strength and form.
Who makes Triesence?
Harrow Eye holds the FDA application for Triesence (NDA022048, approved November 29, 2007). 1 other company (repackagers or distributors) also list Triesence products.
Is there a generic or store brand of Triesence?
Yes. The FDA NDC Directory lists 24 other products with the same active ingredients, strength and form as a Triesence product, 17 of them generic. Ask your pharmacist whether one is right for you.
Has Triesence been recalled?
No recall linked to Triesence products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Triesence is

Each Triesence product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Triamcinolone acetonide · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
triamcinolone acetonide 40 mg/mL
injection, suspension (ophthalmic)		 Triesence 24 products, 16 companies DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Triamcinolone acetonide →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Triesence products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA022048Harrow EyeNovember 29, 20072

Companies that list Triesence

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Triesence products.

Recalls

No recall linked to Triesence products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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