Quick answers
- What is Amzeeq?
- Amzeeq is a brand name of Minocycline hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Amzeeq product in 1 strength and form.
- Who makes Amzeeq?
- Journey holds the FDA application for Amzeeq (NDA212379, approved October 18, 2019).
- Is there a generic or store brand of Amzeeq?
- Other products of Minocycline hydrochloride are listed with the FDA, but none in exactly the same strength and form as a Amzeeq product.
- Has Amzeeq been recalled?
- No recall linked to Amzeeq products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Amzeeq is
Each Amzeeq 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.
Minocycline hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| minocycline hydrochloride 4% aerosol, foam (topical) | Amzeeq | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Minocycline hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA212379 | Journey | October 18, 2019 | 1 |
Companies that list Amzeeq
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Amzeeq products.
- Journey Medical Corporation1 product
Recalls
No recall linked to Amzeeq 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.