Quick answers
- What is Flovent Diskus?
- Flovent Diskus is a brand name of Fluticasone propionate, a prescription medicine. The FDA NDC Directory lists 2 Flovent Diskus products in 2 strengths and forms.
- Who makes Flovent Diskus?
- Glaxo GRP Ltd holds the FDA application for Flovent Diskus (NDA020833, approved September 29, 2000). 1 other company (repackagers or distributors) also list Flovent Diskus products.
- Is there a generic or store brand of Flovent Diskus?
- Yes. The FDA NDC Directory lists 6 other products with the same active ingredients, strength and form as a Flovent Diskus product, 6 of them generic. Ask your pharmacist whether one is right for you.
- Has Flovent Diskus been recalled?
- No recall linked to Flovent Diskus products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Flovent Diskus is
Each Flovent Diskus 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.
Fluticasone propionate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| fluticasone propionate 100 ug powder, metered (respiratory (inhalation)) | Flovent Diskus | 3 products, 3 companies | DailyMed |
| fluticasone propionate 50 ug powder, metered (respiratory (inhalation)) | Flovent Diskus | 3 products, 3 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Fluticasone propionate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020833 | Glaxo GRP Ltd | September 29, 2000 | 2 |
Companies that list Flovent Diskus
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Flovent Diskus products.
- A-S Medication Solutions1 product
- Proficient Rx LP1 product
Recalls
No recall linked to Flovent Diskus 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.