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Brand-name prescription medicine

Triderm

Generic name: Triamcinolone acetonide

FDA application holder: Crown Labs

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

3Strengths and forms
99Same medicine, other names
1984FDA approval
0Recalls (FDA reports)

Quick answers

What is Triderm?
Triderm is a brand name of Triamcinolone acetonide, a prescription medicine. The FDA NDC Directory lists 3 Triderm products in 3 strengths and forms.
Who makes Triderm?
Crown Labs holds the FDA application for Triderm (ANDA088042, approved March 19, 1984).
Is there a generic or store brand of Triderm?
Yes. The FDA NDC Directory lists 99 other products with the same active ingredients, strength and form as a Triderm product, 99 of them generic. Ask your pharmacist whether one is right for you.
Has Triderm been recalled?
No recall linked to Triderm products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Triderm is

Each Triderm 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 0.025%
cream (topical)		 Triderm 20 products, 12 companies DailyMed
triamcinolone acetonide 0.1%
cream (topical)		 Triderm 58 products, 23 companies DailyMed
triamcinolone acetonide 0.5%
cream (topical)		 Triderm 21 products, 12 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

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
FDA applications of Triderm products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
ANDA088042Crown LabsMarch 19, 19843

Companies that list Triderm

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

Recalls

No recall linked to Triderm 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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