Enzeevu — licensed biologic

Overview

Source: Purple Book

Proprietary name

Enzeevu

Proper name

aflibercept-abzv

Licence type

351(k) Biosimilar

BLA number

761382

Applicant

Sandoz 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	August 9, 2024
2MG/0.05ML	Injection	Intravitreal	Pre-Filled Syringe	Rx	August 9, 2024

Reference product

Source: Purple Book

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

View reference product Search the small-molecule catalogue

Sources for this page

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