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:

2019-06-27

Original market date: See footnote 1

2018-06-26

Product name:

M-DULOXETINE

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DIN:

02473208

Product Monograph/Veterinary Labelling:

Date: 2021-11-16 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

MANTRA PHARMA INC
1000 Rue Du Lux Suite 201
Brossard
Quebec
Canada J4Y 0E3

Class:

Human

Dosage form(s):

Capsule (Delayed Release)

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Prescription

 

American Hospital Formulary Service (AHFS): See footnote 3

28:16.04.16 

Anatomical Therapeutic Chemical (ATC): See footnote 4

N06AX21 DULOXETINE

Active ingredient group (AIG) number:See footnote5

0152350001

List of active ingredient(s)
Active ingredient(s) Strength
DULOXETINE (DULOXETINE HYDROCHLORIDE) 30 MG
Version 4.0.2
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