Quick answers
- What is Tridesilon Cream?
- Tridesilon Cream is a brand name of Desonide, a prescription medicine. The FDA NDC Directory lists 1 Tridesilon Cream product in 1 strength and form.
- Who makes Tridesilon Cream?
- Padagis US holds the FDA application for Tridesilon Cream (NDA017010, approved January 4, 1972).
- Is there a generic or store brand of Tridesilon Cream?
- Other products of Desonide are listed with the FDA, but none in exactly the same strength and form as a Tridesilon Cream product.
- Has Tridesilon Cream been recalled?
- No recall linked to Tridesilon Cream products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Tridesilon Cream is
Each Tridesilon Cream 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.
Desonide · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| desonide 0.03 g/60 g cream (topical) | Tridesilon Cream | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Desonide →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA017010 | Padagis US | January 4, 1972 | 1 |
Companies that list Tridesilon Cream
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Tridesilon Cream products.
- Encore Dermatology Inc1 product
Recalls
No recall linked to Tridesilon Cream products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.