Hulio — licensed biologic

Overview

Source: Purple Book

Proprietary name

Hulio

Proper name

adalimumab-fkjp

Licence type

351(k) Interchangeable

BLA number

761154

Applicant

Biocon Biologics Inc.

Center

CDER

Presentations

3

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 also carries the interchangeable designation, so a pharmacist may substitute it for the reference product without contacting 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
20MG/0.4ML	Injection	Subcutaneous	Pre-Filled Syringe	Rx	July 6, 2020
40MG/0.8ML	Injection	Subcutaneous	Autoinjector	Rx	July 6, 2020
40MG/0.8ML	Injection	Subcutaneous	Pre-Filled Syringe	Rx	July 6, 2020

Reference product

Source: Purple Book

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

View reference product Search the small-molecule catalogue

Sources for this page

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