On this page

Avsola

infliximab-axxq

351(k) Biosimilar

Overview

Source: Purple Book
Proprietary name
Avsola
Proper name
infliximab-axxq
Licence type
351(k) Biosimilar
BLA number
761086
Applicant
Amgen Inc.
Center
CDER
Presentations
1
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
100MG For Injection Intravenous Single-Dose Vial Rx December 6, 2019

Reference product

Source: Purple Book

This product is licensed with reference to Remicade (infliximab).

Sources for this page

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