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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:

2013-05-22

Original market date: See footnote 1

1988-12-31

Product name:

PEGLYTE POWDER

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:

00777838

Product Monograph/Veterinary Labelling:

Date: 2015-10-02 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

PENDOPHARM DIVISION OF PHARMASCIENCE INC
100  6111 Royalmount Ave
Montreal
Quebec
Canada  H4P 2T4

Class: 

Human

Dosage form(s):

Powder For Solution

Route(s) of administration:

Oral

Number of active ingredient(s):

5

Schedule(s):

Ethical  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

56:12.00   CATHARTICS AND LAXATIVES

Anatomical Therapeutic Chemical (ATC): See footnote 4

A06AD10  MINERAL SALTS IN COMBINATION

Active ingredient group (AIG) number:See footnote 5

0516978006

List of active ingredient(s)
Active ingredient(s) Strength
MACROGOL 238.18 G / BOTTLE
POTASSIUM CHLORIDE 3.05 G / BOTTLE
SODIUM BICARBONATE 6.76 G / BOTTLE
SODIUM CHLORIDE 5.85 G / BOTTLE
SODIUM SULFATE 22.96 G / BOTTLE

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