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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:

2016-05-03

Original market date: See footnote 1

2016-05-03

Product name:

JAMP-DULOXETINE

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:

02451921

Product Monograph/Veterinary Labelling:

Date: 2020-06-03 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

JAMP PHARMA CORPORATION
1310 Rue Nobel
Boucherville
Quebec
Canada  J4B 5H3

Class: 

Human

Dosage form(s):

Capsule (Delayed Release)

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

28:16.04.16   SELECTIVE SEROTONIN AND NOREPINEPHRINE-REUPTAKE INHIBITORS

Anatomical Therapeutic Chemical (ATC): See footnote 4

N06AX21  DULOXETINE

Active ingredient group (AIG) number:See footnote 5

0152350002

List of active ingredient(s)
Active ingredient(s) Strength
DULOXETINE (DULOXETINE HYDROCHLORIDE) 60 MG

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