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Yusimry

adalimumab-aqvh

351(k) Biosimilar

Overview

Source: Purple Book
Proprietary name
Yusimry
Proper name
adalimumab-aqvh
Licence type
351(k) Biosimilar
BLA number
761216
Applicant
Emerge Bioscience Pte. Ltd.
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
40MG/0.8ML Injection Subcutaneous Pre-Filled Syringe Rx December 17, 2021
40MG/0.8ML Injection Subcutaneous Autoinjector Rx February 27, 2023

Reference product

Source: Purple Book

This product is licensed with reference to Humira (adalimumab).

Sources for this page

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