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:

2014-06-30

Original market date: See footnote 1

1993-12-31

Product name:

SURVANTA

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DIN:

02016109

Product Monograph/Veterinary Labelling:

Date: 2021-06-01 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

ABBVIE CORPORATION
8401 Trans-Canada Highway
Saint-Laurent
Quebec
Canada H4S 1Z1

Class:

Human

Dosage form(s):

Suspension

Route(s) of administration:

Intratracheal

Number of active ingredient(s):

1

Schedule(s):

Prescription

 

American Hospital Formulary Service (AHFS): See footnote 3

48:36.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

R07AA02 NATURAL PHOSPHOLIPIDS

Active ingredient group (AIG) number:See footnote5

0124200001

List of active ingredient(s)
Active ingredient(s) Strength
BERACTANT 25 MG / ML
Version 4.0.2
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