NDC 73606-020

Syfovre 15 mg per 0.1 mL injection, solution

On the label: Apellis Pharmaceuticals, Inc..

Switzerland: 1Japan: 1United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bachem AGBubendorf, SwitzerlandMakes the active ingredient Problems found, fixed voluntarilyAug 16, 2024 · 4 inspections
Juzen Chemical CorporationToyama-city, JapanMakes the active ingredient Problems found, fixed voluntarilyAug 1, 2025 · 6 inspections
Lifecore Biomedical, LLCChaska, MN, United StatesMakes it Problems found, fixed voluntarilyMar 12, 2025 · 4 inspections
Eurofins Advantar Laboratories, LLCSan Diego, CA, United StatesTests it Problems found, fixed voluntarilyJun 30, 2026 · 3 inspections
Eurofins Lancaster Laboratories, LLCLancaster, PA, United StatesTests it Problems found, fixed voluntarilyAug 26, 2025 · 8 inspections
Lifecore Biomedical Operating Company, Inc.Chaska, MN, United StatesTests it Problems found, fixed voluntarilyMar 12, 2025 · 4 inspections
Micro Measurement Laboratories, Inc.Wheeling, IL, United StatesTests it Problems found, fixed voluntarilyApr 28, 2026 · 9 inspections
Packaging Coordinators, LLCPhiladelphia, PA, United StatesPackages it Problems found, fixed voluntarilyJan 31, 2025 · 6 inspections
West Services and Solutions LLCExton, PA, United StatesTests it No problems foundMar 9, 2026 · 5 inspections

Product details

Generic drug
Pegcetacoplan: every company that makes it
Form
injection, solution, intravitreal
Strength
15 mg per 0.1 mL
Approval
NDA NDA217171
On the market since
Feb 17, 2023
Package NDCs
73606-020-01 73606-020-02 73606-020-11 73606-020-12
Official label
DailyMed (National Library of Medicine), updated Sep 16, 2025

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