Quick answers
- What is Trisenox?
- Trisenox is a brand name of Arsenic trioxide, a prescription medicine. The FDA NDC Directory lists 1 Trisenox product in 1 strength and form.
- Who makes Trisenox?
- Cephalon holds the FDA application for Trisenox (NDA021248, approved September 25, 2000).
- Is there a generic or store brand of Trisenox?
- Yes. The FDA NDC Directory lists 8 other products with the same active ingredients, strength and form as a Trisenox product, 8 of them generic. Ask your pharmacist whether one is right for you.
- Has Trisenox been recalled?
- No recall linked to Trisenox products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Trisenox is
Each Trisenox 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.
Arsenic trioxide · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| arsenic trioxide 2 mg/mL injection, solution (intravenous) | Trisenox | 8 products, 7 companies | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Arsenic trioxide →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021248 | Cephalon | September 25, 2000 | 1 |
Companies that list Trisenox
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Trisenox products.
- Cephalon, LLC1 product
Recalls
No recall linked to Trisenox 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.