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:

2012-03-05

Original market date: See footnote 1

1957-12-31

Product name:

PHENOBARB

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:

00178802

Product Monograph/Veterinary Labelling:

Date: 2020-10-02 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):

Tablet

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Schedule G (CDSA IV)

 

American Hospital Formulary Service (AHFS): See footnote 3

28:24.04  ,  28:12.04 

Anatomical Therapeutic Chemical (ATC): See footnote 4

N03AA02 PHENOBARBITAL

Active ingredient group (AIG) number:See footnote5

0105950005

List of active ingredient(s)
Active ingredient(s) See footnote8 Strength
PHENOBARBITAL 30 MG
Version 4.0.3

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