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:

2020-06-15

Original market date: See footnote 1

2020-06-15

Product name:

ARIDOL

Description:

ORAL INHALATION POWDER CAPSULES OF VARYING STRENGTHS, INHALER INCLUDED

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DIN:

02489562

Product Monograph/Veterinary Labelling:

Date: 2019-06-12 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

PHARMAXIS LTD
Locked Bag 5015
Frenchs Forest
New South Wales
Australia 2086

Class:

Human

Dosage form(s):

Powder ,  Kit

Route(s) of administration:

Inhalation

Number of active ingredient(s):

4

Schedule(s):

Prescription Recommended

 

American Hospital Formulary Service (AHFS): See footnote 3

36:00.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

V04CX OTHER DIAGNOSTIC AGENTS

Active ingredient group (AIG) number:See footnote5

0461510001

List of active ingredient(s)
Active ingredient(s) Strength
MANNITOL 10 MG / CAP
MANNITOL 20 MG / CAP
MANNITOL 40 MG / CAP
MANNITOL 5 MG / CAP
Version 4.0.2
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