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Eydenzelt

aflibercept-boav

351(k) Biosimilar

Overview

Source: Purple Book
Proprietary name
Eydenzelt
Proper name
aflibercept-boav
Licence type
351(k) Biosimilar
BLA number
761377
Applicant
CELLTRION, Inc.
Center
CDER
Presentations
2
First licensure
—
351(k) biosimilar pathway. This product was licensed as highly similar to a reference product, with no clinically meaningful differences in safety, purity or potency. It is licensed as a biosimilar but is not designated interchangeable, so substitution requires the prescriber.

Presentations

Source: Purple Book
Every strength and presentation recorded in the Purple Book for this product.
Strength Dosage form Route Presentation Status Licensed
2MG/0.05ML Injection Intravitreal Single-Dose Vial Rx October 2, 2025
2MG/0.05ML Injection Intravitreal Pre-Filled Syringe Rx October 2, 2025

Reference product

Source: Purple Book

This product is licensed with reference to Eylea (aflibercept).

Sources for this page

Purple Book FDA Licence type, presentations, reference product, exclusivity