Product information

From Health Canada

The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Marketed

Current status date:

2024-03-20

Original market date: See footnote 1

2021-02-16

Product name:

HULIO

Description:

SINGLE-DOSE PREFILLED PENS

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section.

DIN:

02502402

Product Monograph/Veterinary Labelling:

Date: 2023-07-20 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

BIOSIMILAR COLLABORATIONS IRELAND LIMITED
UNIT 35/36 Grange Parade, Baldoyle Industrial Estate, Dublin 13
Dublin
--
Ireland D13R20R

Class:

Human

Dosage form(s):

Solution

Route(s) of administration:

Subcutaneous

Number of active ingredient(s):

1

Schedule(s):

Schedule D ,  Prescription

Biosimilar Biologic Drug:

Yes

American Hospital Formulary Service (AHFS): See footnote 3

92:36.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

L04AB04 ADALIMUMAB

Active ingredient group (AIG) number:See footnote5

0150364003

List of active ingredient(s)
Active ingredient(s) See footnote8 Strength
ADALIMUMAB 40 MG / 0.8 ML

Risk Management Plans See footnote 7

A Risk Management Plan (RMP) for this product was submitted.

Pharmacovigilance/Monitoring Activity
Clinical Trials
Observational Studies
Version 4.0.3

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