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:

2022-08-11

Original market date: See footnote 1

2008-04-10

Product name:

OMNARIS

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DIN:

02303671

Product Monograph/Veterinary Labelling:

Date: 2021-02-11 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

COVIS PHARMA GMBH
Grafenauweg 12
Zug
Zug
Switzerland 6300

Class:

Human

Dosage form(s):

Spray, Metered Dose

Route(s) of administration:

Nasal

Number of active ingredient(s):

1

Schedule(s):

Prescription

 

American Hospital Formulary Service (AHFS): See footnote 3

52:08.08 

Anatomical Therapeutic Chemical (ATC): See footnote 4

R01AD13 CICLESONIDE

Active ingredient group (AIG) number:See footnote5

0151669001

List of active ingredient(s)
Active ingredient(s) Strength
CICLESONIDE 50 MCG / ACT
Version 4.0.2
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