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Brand-name prescription medicine

Syfovre

Generic name: Pegcetacoplan

FDA application holder: Apellis Pharms

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 Syfovre?
Syfovre is a brand name of Pegcetacoplan, a prescription medicine. The FDA NDC Directory lists 1 Syfovre product in 1 strength and form.
Who makes Syfovre?
Apellis Pharms holds the FDA application for Syfovre (NDA217171, approved February 17, 2023).
Is there a generic or store brand of Syfovre?
Other products of Pegcetacoplan are listed with the FDA, but none in exactly the same strength and form as a Syfovre product.
Has Syfovre been recalled?
No recall linked to Syfovre products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Syfovre is

Each Syfovre 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.

Pegcetacoplan · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
pegcetacoplan 15 mg/0.1 mL
injection, solution (intravitreal)
Syfovre None listed DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Syfovre products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA217171Apellis PharmsFebruary 17, 20231

Companies that list Syfovre

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

Recalls

No recall linked to Syfovre 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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