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Brand-name prescription medicine

Cometriq

Generic name: Cabozantinib

FDA application holder: Exelixis

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

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 formProduct namesSame medicine, other namesLabel
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.
FDA applications of Cometriq products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA203756ExelixisNovember 29, 20121

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.

Recalls

No recall linked to Cometriq products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. 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.

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