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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:

2005-08-26

Original market date: See footnote 1

1994-12-31

Product name:

HALOPERIDOL LA

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:

02130300

Product Monograph/Veterinary Labelling:

Date: 2013-11-13 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

SANDOZ CANADA INCORPORATED
110 Rue De Lauzon
Boucherville
Quebec
Canada  J4B 1E6

Class: 

Human

Dosage form(s):

Liquid

Route(s) of administration:

Intramuscular

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

28:16.08.08   BUTYROPHENONES

Anatomical Therapeutic Chemical (ATC): See footnote 4

N05AD01  HALOPERIDOL

Active ingredient group (AIG) number:See footnote 5

0101774008

List of active ingredient(s)
Active ingredient(s) Strength
HALOPERIDOL (HALOPERIDOL DECANOATE) 100 MG / ML

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