Quick answers
- What is Kyzatrex?
- Kyzatrex is a brand name of Testosterone undecanoate, a prescription medicine. The FDA NDC Directory lists 3 Kyzatrex products in 3 strengths and forms.
- Who makes Kyzatrex?
- Marius holds the FDA application for Kyzatrex (NDA213953, approved July 27, 2022).
- Is there a generic or store brand of Kyzatrex?
- Other products of Testosterone undecanoate are listed with the FDA, but none in exactly the same strength and form as a Kyzatrex product.
- Has Kyzatrex been recalled?
- No recall linked to Kyzatrex products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Kyzatrex is
Each Kyzatrex 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.
Testosterone undecanoate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| testosterone undecanoate 150 mg capsule, liquid filled (oral) | Kyzatrex | None listed | — |
| testosterone undecanoate 200 mg capsule, liquid filled (oral) | Kyzatrex | None listed | — |
| testosterone undecanoate 50 mg capsule, liquid filled (oral) | Kyzatrex | None listed | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Testosterone undecanoate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA213953 | Marius | July 27, 2022 | 3 |
Companies that list Kyzatrex
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Kyzatrex products.
- Marius Pharmaceuticals3 products
Recalls
No recall linked to Kyzatrex 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.