Quick answers
- What is Nasacort?
- Nasacort is a brand name of Triamcinolone acetonide, an over-the-counter medicine. The FDA NDC Directory lists 2 Nasacort products in 1 strength and form.
- Who makes Nasacort?
- Chattem Sanofi holds the FDA application for Nasacort (NDA020468, approved May 20, 1996). 1 other company (repackagers or distributors) also list Nasacort products.
- Is there a generic or store brand of Nasacort?
- Yes. The FDA NDC Directory lists 27 other products with the same active ingredients, strength and form as a Nasacort product, 27 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Nasacort been recalled?
- No recall linked to Nasacort products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Nasacort is
Each Nasacort 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 · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| triamcinolone acetonide 55 ug spray, metered (nasal) | Nasacort, Nasacort Allergy 24HR | 27 products, 24 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Triamcinolone acetonide →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020468 | Chattem Sanofi | May 20, 1996 | 2 |
Companies that list Nasacort
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Nasacort products.
- A-S Medication Solutions1 product
- Chattem, Inc.1 product
Recalls
No recall linked to Nasacort 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.