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:

2021-11-30

Original market date: See footnote 1

2005-07-05

Product name:

TARO-DOMPERIDONE

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DIN:

02268078

Product Monograph/Veterinary Labelling:

Date: 2021-11-26 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

SUN PHARMA CANADA INC
126 East Drive
Brampton
Ontario
Canada L6T 1C1

Class:

Human

Dosage form(s):

Tablet

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Prescription

 

American Hospital Formulary Service (AHFS): See footnote 3

56:32.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

A03FA03 DOMPERIDONE

Active ingredient group (AIG) number:See footnote5

0116957001

List of active ingredient(s)
Active ingredient(s) Strength
DOMPERIDONE (DOMPERIDONE MALEATE) 10 MG
Version 4.0.2
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