Quick answers
- What is Cometriq?
- Cometriq is a brand name of Cabozantinib, a prescription medicine. The FDA NDC Directory lists 1 Cometriq product in 1 strength and form.
- Who makes Cometriq?
- Exelixis holds the FDA application for Cometriq (NDA203756, approved November 29, 2012).
- Is there a generic or store brand of Cometriq?
- Other products of Cabozantinib are listed with the FDA, but none in exactly the same strength and form as a Cometriq product.
- Has Cometriq been recalled?
- No recall linked to Cometriq products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Cometriq is
Each Cometriq 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.
Cabozantinib · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| cabozantinib s-malate 20 mg capsule (oral) | Cometriq | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Cabozantinib →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA203756 | Exelixis | November 29, 2012 | 1 |
Companies that list Cometriq
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Cometriq products.
- Exelixis, Inc.1 product
Recalls
No recall linked to Cometriq 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.