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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:

2014-01-11

Original market date: See footnote 1

1985-12-31

Product name:

TEVA-LORAZEPAM

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:

00637750

Product Monograph/Veterinary Labelling:

Date: 2019-09-30 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

TEVA CANADA LIMITED
30 Novopharm Court
Toronto
Ontario
Canada  M1B 2K9

Class: 

Human

Dosage form(s):

Tablet

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Targeted (CDSA IV)  

American Hospital Formulary Service (AHFS): See footnote 3

28:24.08   BENZODIAZEPINES

Anatomical Therapeutic Chemical (ATC): See footnote 4

N05BA06  LORAZEPAM

Active ingredient group (AIG) number:See footnote 5

0110731002

List of active ingredient(s)
Active ingredient(s) Strength
LORAZEPAM 2 MG

Application information

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