Quick answers
- What is Bryhali?
- Bryhali is a brand name of Halobetasol propionate, a prescription medicine. The FDA NDC Directory lists 1 Bryhali product in 1 strength and form.
- Who makes Bryhali?
- Bausch holds the FDA application for Bryhali (NDA209355, approved November 6, 2018).
- Is there a generic or store brand of Bryhali?
- Other products of Halobetasol propionate are listed with the FDA, but none in exactly the same strength and form as a Bryhali product.
- Has Bryhali been recalled?
- No recall linked to Bryhali products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Bryhali is
Each Bryhali 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.
Halobetasol propionate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| halobetasol propionate 0.01% lotion (topical) | Bryhali | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Halobetasol propionate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA209355 | Bausch | November 6, 2018 | 1 |
Companies that list Bryhali
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Bryhali products.
- Bausch Health US, LLC1 product
Recalls
No recall linked to Bryhali 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.