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Brand-name prescription medicine

Rizafilm

Generic name: Rizatriptan benzoate

FDA application holder: Gensco

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 Rizafilm?
Rizafilm is a brand name of Rizatriptan benzoate, a prescription medicine. The FDA NDC Directory lists 3 Rizafilm products in 2 strengths and forms.
Who makes Rizafilm?
Gensco holds the FDA application for Rizafilm (NDA205394, approved April 14, 2023). 1 other company (repackagers or distributors) also list Rizafilm products.
Is there a generic or store brand of Rizafilm?
Other products of Rizatriptan benzoate are listed with the FDA, but none in exactly the same strength and form as a Rizafilm product.
Has Rizafilm been recalled?
No recall linked to Rizafilm products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Rizafilm is

Each Rizafilm 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.

Rizatriptan benzoate · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
rizatriptan benzoate 10 mg
film (oral)
Rizafilm None listed DailyMed
rizatriptan benzoate 5 mg
film (oral)
Rizafilm None listed DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Rizatriptan benzoate →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Rizafilm products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA205394GenscoApril 14, 20233

Companies that list Rizafilm

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Rizafilm products.

Recalls

No recall linked to Rizafilm 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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